Wearable protective massage device
By designing an unlockable and locking structure for the penile protective shield and testicular locking assembly, combined with mesh breathability and vibration function, the problems of unstable fixation, poor breathability and liquid accumulation in existing protective devices are solved, achieving multiple effects of stable wearing, hygiene and rehabilitation stimulation.
Patent Information
- Application Number
- CN202511383096.9
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-09-24
- Publication Date
- 2025-12-16
AI Technical Summary
Existing protective devices have drawbacks during male circumcision, urethral infection treatment, herpes treatment, or other genital area postoperative recovery. These drawbacks include poor fixation, poor breathability, inability to urinate, easy accumulation of fluid or sweat inside, and lack of active drainage or rehabilitation stimulation mechanisms, leading to the risk of muscle atrophy and bacterial growth.
A wearable protective massage device has been designed, including a penile shield, a testicular locking assembly, and a vibration assembly. It is fixed to the base of the scrotum through an unlockable locking structure. Combining the breathability of the mesh structure and the vibration function, it realizes the drainage and discharge of liquid. It is also equipped with remote control and personalized adjustment to ensure a secure fit and hygiene.
It effectively prevents detachment and friction, keeps the affected area dry and hygienic, promotes blood circulation and muscle relaxation, improves ease of use and hygiene, adapts to different physiological conditions, and reduces the risk of bacterial growth.
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Figure CN121129541A_ABST
Abstract
Description
TECHNICAL FIELD
[0001] The present application relates to the technical field of protective and rehabilitation devices, in particular to a wearable protective massage device. BACKGROUND
[0002] In the postoperative recovery process of male foreskin surgery, urethral infection treatment, herpes treatment or other genital area, it is usually necessary to isolate and protect the affected area to avoid friction with external trousers causing wound tearing or infection. The existing protection means mostly uses gauze bandaging or ordinary sheath, which has the problems of poor fixation, poor air permeability, inability to urinate, easy accumulation of liquid or sweat inside, etc. Long-term wearing may also cause muscle atrophy or discomfort.
[0003] In addition, the existing protective device has single function, lacks active liquid drainage or rehabilitation stimulation mechanism, and the inside is damp after the user takes a bath or uses the toilet, which is difficult to handle and easy to breed bacteria. Although some products have locking structures, they lack reliable lock design and anti-dropping mechanism that conforms to ergonomics, and are difficult to maintain stable wearing in the active state.
[0004] Therefore, it is necessary to provide an integrated protective device that can realize reliable fixation, has liquid diversion and drainage function, and can provide moderate rehabilitation stimulation, to meet the multiple needs of postoperative protection, sanitary maintenance and rehabilitation training. SUMMARY
[0005] The purpose of the present application is to solve the above problems, provide a wearable protective massage device, which can meet the needs of postoperative protection and rehabilitation training of users, and improve the above problems.
[0006] The present application is realized by the following technical scheme: The present application provides a wearable protective massage device, which comprises a penis protective cover, a testicle lock assembly and a vibration assembly. The penis protective cover is provided with a first lock connection part. The testicle lock assembly is provided with a second lock connection part. The penis protective cover is formed by a shell with a net-like or local net-like structure, and an internal cavity for accommodating the penis is formed inside. The first lock connection part and the second lock connection part are locked to each other in an unlockable manner. When the first lock connection part and the second lock connection part are in the locked state, a closed narrow gap is formed between the testicle lock assembly and the penis protective cover, which is used to hold the root of the scrotum. The size of the closed narrow gap is configured to prevent the scrotum from slipping. The vibration assembly is arranged inside and / or connected to the penis protective cover.
[0007] The technical scheme of the embodiment of the application is characterized in that the first locking part and the second locking part are locked, and the closed narrow gap clamps the root of the scrotum, so that the whole device is firmly fixed on the human body, effectively avoiding falling off and displacement caused by daily activities (such as walking and running). The hard penis protection cover shell can perfectly isolate the direct contact and friction between the penis and clothes, providing essential physical protection for the postoperative wound or sensitive area, greatly reducing the discomfort of the user. The size of the closed narrow gap can tightly clamp the skin of the root of the scrotum without excessive compression to cause discomfort, fundamentally preventing the scrotum from accidentally slipping out of the gap, and ensuring the functionality and safety of the device. The mesh or partial mesh structure of the penis protection cover ensures air circulation in the cavity, avoiding stuffiness and dampness in a completely closed environment, which is conducive to keeping the affected area dry and hygienic, and reducing the risk of bacterial growth. After bathing or cleaning, the vibration assembly can generate a gentle vibration. The vibration can effectively shake off water droplets attached to the inner wall of the protection cover and the surface of the penis, guide the liquid to flow downward to the opening for discharge, and assist in accelerating the drying process, solving the problem of difficult to wipe off the internal liquid; in addition, the vibration applied to the user's penis by the vibration assembly can promote blood circulation and muscle relaxation in the user's penis, avoiding muscle atrophy caused by long-term non-use.
[0008] In some embodiments, a remote control end and a wireless control assembly are further included; the wireless control assembly has a first communication unit and a second communication unit; wherein the vibration assembly has a driving control end; wherein the first communication unit and the second communication unit are respectively arranged on the remote control end and the driving control end, and are used to transmit at least a control signal from the remote control end.
[0009] In the technical scheme of the embodiment of the application, non-contact control is realized through the remote control end and the wireless control assembly, so that the user can operate without directly contacting the device, which is particularly important during the sensitive period after surgery or when the hands are unclean, and improves the convenience and hygiene level of use. The problem of difficult physical button operation caused by inconvenient device wearing position is overcome. The user can flexibly control the vibration function within a certain distance, for example, without having to search for the body switch after bathing, and directly starting the water removal mode through the remote control end.
[0010] In some embodiments, the cavity has a first opening and a second opening; wherein the cavity is a long strip structure with a cross section approximating a circle perpendicular to the length direction; wherein the first opening and the second opening are respectively located at both ends of the length direction of the cavity; wherein the length direction of the cavity is the axis direction of the long strip structure of the cavity; and wherein the first locking part is arranged at the first opening.
[0011] In the technical solution of this application embodiment, the larger first opening provides a spacious entrance, allowing the user to easily and quickly insert the penis into the cavity, avoiding wearing difficulties or friction discomfort caused by an excessively small entrance, thus improving the user experience. The cavity adopts a long strip-shaped structure extending along the axis with an approximately circular cross-section, which best conforms to the natural shape of the human penis, providing uniform containment and support, minimizing the feeling of foreign objects and pressure during wear, and improving wearing comfort. The first locking part is located at the first opening, so that the connection point between the testicular locking assembly and the main body is located at the base of the penis. This position provides structural stability and reasonable force distribution, ensuring the firmness after locking, while also making the overall structural layout compact and reasonable.
[0012] In some embodiments, the diameter of the second opening is 1 / 5 to 1 / 2 of the diameter of the first opening.
[0013] In the technical solution of this application embodiment, the design of the size of the second opening ensures smooth urination, avoiding urine splashing or blockage caused by an excessively small opening, while also preventing the loss of its guiding and protective functions due to an excessively large opening. The smaller second opening increases the difficulty of accidental slippage of the penis from the front, and together with the closed narrow slit at the base and the locking part, it forms a dual anti-slip mechanism, improving the safety and reliability of the device during strenuous activity or nighttime wear. Compared to a large-diameter opening, the smaller second opening generates better capillary action and confluence during vibration-induced drainage, helping to collect droplets and allow them to drip more efficiently under gravity, accelerating internal drying and maintaining hygiene.
[0014] In some embodiments, the penis shield is provided with a draining portion near the second opening; the draining portion is configured to collect surrounding liquid and gather it into droplets when the user wears it standing up, and to cause the droplets to fall.
[0015] In the technical solution of this application embodiment, the draining section actively collects and removes residual liquid, solving the problem of the last few drops in the droplets being difficult to handle, promoting the final drying of the device, avoiding the growth of bacteria in a humid environment, and improving the hygiene level of use; by guiding the liquid to be discharged in an orderly manner in the form of dripping, the draining section effectively prevents the liquid from flowing disorderly and wetting clothes or the user's groin, keeping the body and clothes dry and clean.
[0016] In some embodiments, a first size adjustment component is further included, which is used to adjust the length of the cavity.
[0017] In the technical solution of this application embodiment, the first size adjustment component allows users to flexibly adjust the cavity length according to their real-time physiological state (such as postoperative swelling or normal state) or personal comfort preferences, achieving personalized customization and ensuring the best wearing experience. By shortening the cavity length, the relative position of the urethral opening and the second opening during urination is optimized, playing a role in assisting alignment. This significantly reduces the possibility of urine accumulation in the cavity, improving the hygiene and convenience of the device. The wearable protective massage device provided by this application, through its adjustable design, can adapt to a wide range of users with different heights and physiological conditions, avoiding the need to produce multiple fixed-size specifications and enhancing product versatility.
[0018] In some embodiments, the penile shield includes a first segment and a second segment arranged sequentially along the axial direction of the cavity; a first opening is provided in the first segment and a second opening is provided in the second segment; the second segment is sleeved on the first segment, and a first size adjustment component is provided between the first segment and the second segment; the first size adjustment component is used to control the second segment to slide or be fixed relative to the first segment along the axial direction of the cavity to adjust the length of the cavity.
[0019] In the technical solution of this application embodiment, the structure of the second segment fitted onto the first segment ensures that the two shell segments remain tightly fitted and coaxially aligned throughout the entire adjustment process, preventing shaking or misalignment during adjustment and ensuring the integrity and stability of the structure. Throughout the adjustment process, the cavity remains a continuous cavity composed of the two shell segments, only changing in axial length. This maintains the device's wrapping and protective function for the penis, preventing any gaps that could pinch the skin or leak fluid during adjustment.
[0020] In some embodiments, an elastic positioning ring is provided around the second opening on the inner side of the cavity; the positioning ring is used to contact the tip of the penis so that the urethral opening is aligned with the second opening.
[0021] In the technical solution of this application embodiment, the elastic positioning ring achieves rapid and precise positioning of the penile head within the cavity through physical contact and flexible wrapping. Its core function is to ensure precise alignment between the urethral opening and the second opening. This optimizes urination function, allowing urine to flow directly from the center of the second opening, reducing the risk of urine splashing onto the cavity wall and improving hygiene. Compared to direct contact with the rigid second opening, the elastic positioning ring provides soft cushioning, significantly increasing comfort and avoiding pressure and discomfort that may be caused by hard edges, making it especially suitable for sensitive areas after surgery. The deformable properties of the elastic material allow a single positioning ring to adapt to the physiological size differences of different users, ensuring the universality and effectiveness of the positioning function.
[0022] In some embodiments, the first size adjustment component is configured to control the second segment to slide until the tip of the penis extends into and is limited by the positioning ring, so that the urethral opening is aligned with the second opening.
[0023] In the technical solution of this application embodiment, the length adjustment function is associated with the urethral opening positioning function. Users do not need to observe visually or repeatedly try; they can reliably achieve the key goal of "urethral opening aligned with the second opening" simply through simple sliding adjustment and clear tactile feedback. This simplifies the operation, reduces preparation time for urination, and improves user comfort. The "limiting" function of the positioning ring provides users with a clear and intuitive physical feedback signal (tactile sensation). This makes operation simple and user-friendly, improving user experience and operational reliability. Regardless of how the user adjusts, the final stopping position is determined by the interaction between their own physiological structure and the positioning ring. This ensures that for a specific user, the unique optimal urethral opening alignment position is automatically reproduced each time the ring is worn, guaranteeing consistent functional performance.
[0024] In some embodiments, the inner surface of the cavity has a flow guiding component; the flow guiding component is a flow guiding groove and / or a flow guiding texture.
[0025] In the technical solution of this application embodiment, the flow guiding component actively provides a flow path for the liquid, overcoming the problem of liquid easily spreading and adhering on flat or simple curved surfaces, transforming disordered droplets into orderly flow, and accelerating the speed and efficiency of liquid discharge. By guiding residual liquid from various parts of the cavity to the outlet for centralized discharge, the flow guiding component reduces the situation where individual areas are difficult to dry due to liquid retention, achieving more comprehensive and faster drying inside the cavity, and improving the hygiene level of use.
[0026] In some embodiments, the outer surface of the penile shield is provided with a draining portion; the flow guiding component is configured to guide the liquid in the cavity to the draining portion.
[0027] In the technical solution of this application embodiment, the flow guiding component inside the cavity ensures that the liquid can be quickly collected and discharged from the cavity, while the externally provided drainage and drip-collecting part ensures that the discharged liquid can be effectively treated without wetting the user. The two work together to accelerate the overall drying process and improve hygiene.
[0028] In some embodiments, a vibration control program is also included for driving the vibration assembly to perform water removal vibration and automatically stopping after a rated time has been reached.
[0029] In the technical solution of this application embodiment, the vibration control program encapsulates the water removal function into a one-button triggered automated process. Users do not need to master complex operations or timing, greatly simplifying the usage steps. The mechanism of automatically stopping after the rated time avoids the vibration component running idle for a long time due to the user forgetting to turn it off, effectively saving battery power and preventing the motor from being shortened in life due to overheating or prolonged operation. The wearable protective massage device provided by this application solidifies the water removal process through the vibration control program, ensuring that the water removal effect of each vibration is consistent and reliable, avoiding differences in effect caused by varying lengths of manual operation by the user.
[0030] In some embodiments, water removal vibration refers to the alternating switching of the vibration component between a vibration state and a stop state to achieve effective collection and discharge of liquid.
[0031] In the technical solution of this application embodiment, this dynamic-static combination mode is more efficient than continuous vibration. The vibration state is responsible for shaking the liquid off the surface, while the stationary state provides the liquid with the necessary settling time to flow and collect naturally under gravity. The alternation of the two simulates the optimal physical process of slapping and flowing, which can remove liquid faster and more thoroughly. Intermittent operation makes the total running time of the motor much shorter than continuous vibration, significantly reducing power consumption, extending the battery's single-use time, and meeting the energy-saving requirements of wearable devices. The short-duration, intermittent vibration mode avoids the numbness or discomfort that may be caused to sensitive parts by long-term continuous vibration, improving the user experience.
[0032] In some embodiments, a key is also included, which is used to unlock the locking state between the first locking part and the second locking part.
[0033] In the technical solution of this application embodiment, the presence of a key prevents the device from being arbitrarily opened, ensuring its stability and tamper-proof nature during wear. This is particularly suitable for medical scenarios, preventing patients from prematurely removing the device due to discomfort, which could affect postoperative recovery, and enabling authorized management controlled by nursing staff. The reliable mechanical locking structure avoids the risk of accidental opening due to accidental impacts or snagging in daily life, improving safety. Simultaneously, for users who need to wear the device long-term, this design, which allows unauthorized opening, provides a stable sense of psychological security. The purely mechanical key unlocking method does not rely on electricity, signals, or complex procedures, and can work instantly and reliably in any environment (such as a damp bathroom), ensuring absolute functional availability.
[0034] In some embodiments, the second locking portion is configured to adjust its locking position with the first locking portion to adjust the diameter of the closed slit accordingly.
[0035] In the technical solution of this application embodiment, by adjusting the locking position, the user can precisely adjust the actual diameter of the closed narrow slit according to their own physiological structure and comfort perception. This solves the common contradiction of being too tight and uncomfortable or too loose and easy to slip off due to individual differences, realizes personalized customization, and improves the user experience.
[0036] Additional aspects and advantages of this application will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of this application. Attached Figure Description
[0037] To more clearly illustrate the technical solutions of the embodiments of this application, the accompanying drawings used in the embodiments will be briefly introduced below. It should be understood that the following drawings only show some embodiments of this application and should not be regarded as a limitation of the scope. For those skilled in the art, other related drawings can be obtained based on these drawings without creative effort.
[0038] Figure 1 A side view of a wearable protective massage device provided in some embodiments of this application; Figure 2 This is a schematic diagram of the structure of a wearable protective massage device provided in some embodiments of this application; Figure 3 Schematic diagrams of the wearable protective massage device provided in other embodiments of this application; Figure 4 This is a schematic diagram of the structure of a penile shield provided in some embodiments of this application; Figure 5 This is a schematic diagram of the structure of a testicular locking assembly provided in some embodiments of this application; Figure 6 Cross-sectional views of wearable protective massage devices provided in some embodiments of this application; Figure 7 A side view of a wearable protective massage device with a draining section provided in some embodiments of this application; Figure 8 Schematic diagrams of the structure of the first and second segments provided for some embodiments of this application; Figure 9 for Figure 8 Enlarged view of point A in the middle; Figure 10 Structural diagrams of the first and second segments provided for other embodiments of this application; Figure 11 Cross-sectional views of the first and second segments provided for some embodiments of this application; Figure 12 Schematic diagrams of the first and second segments provided for further embodiments of this application; Figure 13 Cross-sectional views of the first and second segments provided for other embodiments of this application; Figure 14 Cross-sectional views of the first and second paragraphs provided for some embodiments of this application Figure 15 A partial structural schematic diagram of a penis shield provided in some embodiments of this application; Figure 16 Schematic diagrams of the flow guiding components and the flow-collecting dripping parts provided in some embodiments of this application; Figure 17 A schematic diagram of the structure of a wearable protective massage device provided in some embodiments of this application when the actual diameter of a closed narrow slit is enlarged; Figure 18 A cross-sectional view of a wearable protective massage device provided in some embodiments of this application when the actual diameter of a closed narrow slit is enlarged; Figure 19 This is a schematic diagram of the structure of a testicular locking assembly with an adjustable locking position provided in some embodiments of this application.
[0039] Icons: 1. Penis protective shield; 10. First locking part; 11. Cavity; 110. First opening; 111. Second opening; 112. Positioning ring; 113. Flow guiding assembly; 12. Inner cavity; 13. Drip collection part; 14. First section; 15. Second section; 2. Testicular locking assembly; 20. Second locking part; 3. Vibration assembly; 30. First vibrating element; 31. Second vibrating element; 4. Closing slit; 5. First size adjustment assembly; 50. Slide; 51. Sliding block; 52. Positioning groove; 53. Positioning protrusion; 54. Positioning pin. Detailed Implementation
[0040] To make the objectives, technical solutions, and advantages of the embodiments of this application clearer, the technical solutions of the embodiments of this application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of this application, not all embodiments. Based on the embodiments of this application, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of this application.
[0041] Unless otherwise defined, all technical and scientific terms used in this application have the same meaning as commonly understood by one of ordinary skill in the art to which this application pertains; the terminology used in the description of this application is for the purpose of describing particular embodiments only and is not intended to limit the application; the terms "comprising" and "having," and any variations thereof, in the description, claims, and accompanying drawings of this application are intended to cover non-exclusive inclusion. The terms "first," "second," etc., in the description, claims, or accompanying drawings of this application are used to distinguish different objects, not to describe a specific order or hierarchy.
[0042] In this application, the reference to "embodiment" means that a specific feature, structure, or characteristic described in connection with an embodiment may be included in at least one embodiment of this application. The appearance of this phrase in various places throughout the specification does not necessarily refer to the same embodiment, nor is it a mutually exclusive, independent, or alternative embodiment. It will be explicitly and implicitly understood by those skilled in the art that the embodiments described in this application can be combined with other embodiments.
[0043] In the description of this application, it should be noted that, unless otherwise expressly specified and limited, the terms "installation," "connection," "linking," and "attachment" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; they can refer to a direct connection or an indirect connection through an intermediate medium; and they can refer to the internal communication between two components. Those skilled in the art can understand the specific meaning of the above terms in this application according to the specific circumstances.
[0044] In this application, the term "and / or" is merely a description of the relationship between related objects, indicating that three relationships can exist. For example, A and / or B can represent: A existing alone, A and B existing simultaneously, or B existing alone. Additionally, in this application, the character " / " generally indicates that the preceding and following related objects have an "or" relationship.
[0045] In this application, "multiple" refers to two or more (including two), similarly, "multiple sets" refers to two or more (including two sets), and "multiple pieces" refers to two or more (including two pieces).
[0046] According to some embodiments of this application, optionally, such as Figures 1-6As shown, this application provides a wearable protective massage device, which includes a penile shield 1, a testicular locking assembly 2, and a vibration assembly 3. The penile shield 1 is provided with a first locking part 10; the testicular locking assembly 2 is provided with a second locking part 20; the penile shield 1 is formed by a shell with a mesh or partially mesh structure, and its interior forms a cavity 11 for accommodating the penis; the first locking part 10 and the second locking part 20 are locked to each other in an unlockable manner; when the first locking part 10 and the second locking part 20 are in the locked state, a closed narrow slit 4 is formed between the testicular locking assembly 2 and the penile shield 1, the closed narrow slit 4 is used to clamp the base of the scrotum, and the size of the closed narrow slit 4 is configured to prevent the scrotum from slipping off; the vibration assembly 3 is disposed inside the penile shield 1 and / or connected to the penile shield 1.
[0047] When the penile shield 1 has a partial mesh structure, the mesh structure of the penile shield 1 is located at the bottom of the cavity 11, allowing the liquid in the cavity 11 to be discharged more easily.
[0048] The inner surface of the cavity 11 can be coated with a hydrophobic coating or made directly with hydrophobic materials. This makes it more difficult for liquids (water, urine) to adhere to the inner wall. Under the action of vibration and gravity, they can bead up and roll off more quickly, improving the ease of cleaning and hygiene of the device.
[0049] The vibration component 3 can be embedded in the inner wall of the penile shield 1 (such as the top or sides), and its vibration can be directly transmitted to the internal cavity 11. Alternatively, it can be placed externally and tightly connected to the outer surface of the penile shield 1, and the vibration can be indirectly transmitted through the vibrating shell.
[0050] To ensure suitability for users of different body types, the second locking part 20 can be designed with multiple locking points (e.g., multiple slots or holes). By changing the specific locking positions of the second locking part 20 and the first locking part 10, the actual diameter of the closed slit 4 can be fine-tuned, thereby achieving a more personalized fit and ensuring both effective anti-slip and comfortable fit.
[0051] Male users who have just undergone genital surgery need to protect this area to avoid postoperative infection and reduce pain caused by clothing friction. The user first slips the testicular locking assembly 2 through the penis and places it inside the scrotum. Then, the penis shield 1 is placed over the penis, ensuring it is fully contained within the cavity 11 formed by the mesh structure shell. The mesh structure ensures basic ventilation. The user then aligns and locks the second locking part 20 on the testicular locking assembly 2 with the first locking part 10 located at the opening end of the penis shield 1. When locked, a closed narrow slit 4 naturally forms between the penis shield 1 and the testicular locking assembly 2. When the user locks the first locking part 10 to the second locking part 20, the closed narrow slit 4 between the penis shield 1 and the testicular locking assembly 2 is tightly clamped at the base of the scrotum, completing the wearing of the device. After showering, water may remain inside the cavity 11. The user can activate the vibration component 3 via the switch on the device or a remote control (if provided). Vibration component 3 generates gentle vibrations.
[0052] Through the locking of the first locking part 10 and the second locking part 20, and the clamping of the scrotum base by the closed narrow slit 4, the entire device is firmly fixed to the human body, effectively preventing it from falling off or shifting due to daily activities (such as walking and running). The rigid outer shell of the penile protective shield 1 perfectly isolates the penis from direct contact and friction with clothing, providing crucial physical protection for postoperative wounds or sensitive areas, greatly reducing user discomfort. The size of the closed narrow slit 4 tightly clamps the skin at the base of the scrotum without excessive pressure causing discomfort, fundamentally preventing the scrotum from accidentally slipping out of the gap, ensuring the functionality and safety of the device. The mesh or partial mesh structure of the penile protective shield 1 ensures air circulation within the cavity 11, avoiding stuffiness and humidity in a completely sealed environment, which helps keep the affected area dry and hygienic, reducing the risk of bacterial growth. After bathing or cleaning, activating the vibration component 3 can generate gentle vibration. The vibration effectively shakes off water droplets adhering to the inner wall of the protective cover and the surface of the penis, guiding the liquid downwards to the opening for discharge, thus accelerating the drying process and solving the problem of difficult-to-wipe internal fluid accumulation. In addition, the vibration component 3 applies vibration to the user's penis, which can promote blood circulation and muscle relaxation inside the penis, preventing muscle atrophy caused by long-term disuse.
[0053] In the specific implementation process, such as Figure 5 As shown, the testicular locking assembly 2 is a circular structure. The width of the part of the circular structure that contacts the user's scrotum is greater than the width of the other parts, and the surface of this part is provided with a wavy textured surface, which can fit and conform to the skin of the user's scrotum.
[0054] According to some embodiments of this application, optionally, a remote control terminal and a wireless control component are also included; the wireless control component has a first communication unit and a second communication unit; wherein the vibration component 3 has a drive control terminal; wherein the first communication unit and the second communication unit are respectively disposed on the remote control terminal and the drive control terminal, for at least transmitting control signals from the remote control terminal.
[0055] The remote control can be a physical remote control with simple buttons specifically developed for the device, or an application running on a smart mobile device such as a smartphone or tablet.
[0056] After wearing the device, the user (either the patient or a caregiver) does not need to directly touch the device if vibration is required (e.g., to assist with drying after bathing or to provide timed rehabilitation stimulation). The user operates a remote control terminal (which can be a dedicated remote control or a smartphone with a control program installed). The first communication unit (such as a Bluetooth module) inside the remote control terminal converts the corresponding control commands into wireless signals and transmits them. The second communication unit installed on the device's drive control terminal receives this wireless signal, and the drive control terminal then decodes the signal and controls the vibration component 3 to perform the corresponding actions (such as starting, stopping, or switching vibration modes). Non-contact control is achieved through a remote control terminal and wireless control components, allowing users to operate the device without direct contact. This is especially important during post-operative sensitive periods or when hands are unclean, improving ease of use and hygiene. It overcomes the difficulty of operating physical buttons due to inconvenient device placement. Users can flexibly control the vibration function from a certain distance; for example, after showering, there's no need to search for the power switch on the device; the dewatering mode can be activated directly through the remote control terminal.
[0057] When the remote control terminal is a smart device app, data recording and intelligent reminder functions can be further developed. The app can record the pattern and duration of each vibration usage and generate a health report based on this data. Simultaneously, it can proactively remind users to perform rehabilitation training or inform them that the device has been worn continuously for too long and requires attention to hygiene, thus enhancing the product's health management functions.
[0058] According to some embodiments of this application, optionally, such as Figure 6 As shown, the cavity 11 has a first opening 110 and a second opening 111; wherein, the cavity 11 is a long strip structure with an approximately circular cross-section extending perpendicular to its length direction; wherein, the first opening 110 and the second opening 111 are respectively located at both ends of the length direction of the cavity 11; wherein, the length direction of the cavity 11 is the axial direction of the long strip of the cavity 11; wherein, the first locking part 10 is provided at the first opening 110.
[0059] The primary function of the first opening 110 is "entry" (wearing entrance and root fixation position), and its size is usually relatively large; while the primary function of the second opening 111 is "exit" (urination and fluid discharge outlet). Together, these two openings form a channel that allows penile insertion and the realization of basic physiological functions.
[0060] The larger first opening 110 provides a spacious entrance, allowing users to easily and quickly insert the penis into the cavity 11, avoiding wearing difficulties or friction discomfort caused by an insufficiently small entrance, thus improving the user experience. The cavity 11 adopts a long strip-shaped structure extending along the axis with an approximately circular cross-section, which best conforms to the natural shape of the human penis, providing uniform containment and support, minimizing the feeling of foreign objects and pressure during wear, and improving wearing comfort. The first locking part 10 is located at the first opening 110, so that the connection point between the testicular locking assembly 2 and the main body is located at the base of the penis. This position provides structural stability and reasonable force distribution, ensuring the firmness after locking, while also making the overall structural layout compact and reasonable.
[0061] In practice, a removable soft plug can be designed at the second opening 111. During non-urination periods, the user can insert the plug to more effectively prevent external contaminants (such as dust and clothing fibers) from entering the cavity 11, thus improving hygiene. When urination is needed, it can be easily removed, combining convenience and protection.
[0062] According to some embodiments of this application, optionally, such as Figure 6 As shown, the diameter of the second opening 111 is 1 / 5 to 1 / 2 of the diameter of the first opening 110.
[0063] When the user wears the device, the base of the penis enters the cavity 11 through the larger first opening 110. After wearing, the tip and glans of the penis are naturally positioned near the end close to the second opening 111. When the user urinates, urine flows out from the urethra. Because the diameter of the second opening 111 is precisely designed to be 1 / 5 to 1 / 2 the diameter of the first opening 110, this size matches the natural distance of the adult urethral opening and the characteristics of urine flow rate. The urine stream can pass smoothly, while the edge of the second opening 111 can naturally conform to the skin surface of the tip of the penis.
[0064] By designing the size of the second opening 111, smooth urination is ensured, preventing urine splashing or blockage due to an excessively small opening, while also avoiding the loss of its drainage and protective functions due to an excessively large opening. The smaller second opening 111 increases the difficulty of accidental slippage of the penis from the front, forming a dual anti-slip mechanism together with the closed narrow slit 4 at the base and the locking part, improving the safety and reliability of the device during strenuous activity or nighttime wear. Compared to a large-diameter opening, the smaller second opening 111 generates better capillary action and confluence during vibration drainage, helping to collect droplets and make them drip more efficiently under gravity, accelerating internal drying and maintaining hygiene.
[0065] According to some embodiments of this application, optionally, such as Figure 7 As shown, the penis shield 1 has a draining part 13 near the second opening 111; the draining part 13 is configured to collect surrounding liquid and form droplets when the user wears it while standing, and to cause the droplets to fall.
[0066] The confluence and dripping section 13 can be a smooth, downwardly convex curved surface formed by the shell in that area, or it can be a local small conical point. Its core functional feature is that its geometry can disrupt the surface tension of water, causing dispersed water droplets to converge towards it and reach the critical volume that allows them to drip naturally.
[0067] After showering or cleaning, although vibration has shaken off most of the water in the cavity 11, some small water droplets or residual liquid may still adhere to the edge and surrounding area of the second opening 111. Because the penile shield 1 has a draining section 13 near the second opening 111 (this section can be a slightly downward-convex smooth surface or a small point), these residual liquids will naturally converge along the outer wall of the shield towards this lowest point (i.e., the draining section 13) under the action of surface tension. When enough liquid gathers at the draining section 13, it will coalesce into a larger droplet. Once the weight of the droplet exceeds the adhesion force (surface tension) between it and the surface of the draining section 13, the droplet will detach on its own, dripping down.
[0068] The drip collection section 13 actively collects and removes residual liquid, solving the problem of the last few drops being difficult to handle, promoting the final drying of the device, preventing bacteria from growing in a damp environment, and improving the hygiene level of use; by guiding the liquid to be discharged in an orderly manner in the form of drips, the drip collection section 13 effectively prevents the liquid from flowing disorderly and wetting clothes or the user's groin, keeping the body and clothes dry and clean.
[0069] In practical implementation, a superhydrophobic (lotus effect) coating can be applied to the dripping section 13 and its surrounding area. This reduces the contact area and adhesion between the liquid and the section, making it easier for droplets to converge and slide off. Even slight vibrations or tilting can cause the droplets to fall quickly, thereby further improving the confluence efficiency and drying speed.
[0070] The drain section 13 can be designed as a removable and installable soft silicone component. Users can periodically remove it for thorough cleaning or replacement, which helps maintain optimal drain performance and personal hygiene.
[0071] According to some embodiments of this application, optionally, such as Figures 8-14 As shown, it also includes a first size adjustment component 5, which is used to adjust the length of the cavity 11.
[0072] The first size adjustment component 5 can be designed as a stepless adjustment that can be locked at any position on the slide rail, or it can be designed as a graded adjustment with several fixed locking positions.
[0073] The first size adjustment component 5 can be a mechanical buckle that requires manual pressing to unlock and then sliding, or it can be a knob that drives a threaded or worm gear structure by rotation.
[0074] After undergoing genital surgery, the user wears the wearable protective massage device provided in this application. Since the penis may be quite swollen in the early postoperative period, the user first adjusts the length of the cavity 11 to its maximum to provide ample space and avoid compressing the wound. After a period of time, as the swelling subsides, the user desires a more snug fit. The user can operate the first size adjustment component 5 located on the penile shield 1 to shorten the overall length of the cavity 11, making it more compatible with the current penis size and improving stability and comfort. When the user needs to urinate, the length of the cavity 11 can be slightly shortened using the first size adjustment component 5. This brings the user's urethral opening closer to the second opening 111, allowing for more accurate aiming during urination and effectively reducing the risk of urine splashing into the cavity 11.
[0075] The first size adjustment component 5 allows users to flexibly adjust the length of the cavity 11 according to their real-time physiological state (such as postoperative swelling or normal state) or personal comfort preferences, achieving personalized customization and ensuring the best wearing experience. By shortening the length of the cavity 11, the relative position of the urethral opening and the second opening 111 during urination is optimized, which plays a role in assisting alignment. This significantly reduces the possibility of urine accumulation in the cavity 11, improving the hygiene and convenience of the device. The wearable protective massage device provided in this application, through its adjustable design, can adapt to a wide range of users with different heights and physiological conditions, avoiding the need to produce multiple fixed-size specifications and enhancing product versatility.
[0076] According to some embodiments of this application, optionally, such as Figures 8-14 As shown, the penile shield 1 includes a first segment 14 and a second segment 15 arranged sequentially along the axial direction of the cavity 11; a first opening 110 is disposed in the first segment 14, and a second opening 111 is disposed in the second segment 15; the second segment 15 is fitted onto the first segment 14, and a first size adjustment component 5 is disposed between the first segment 14 and the second segment 15; the first size adjustment component 5 is used to control the second segment 15 to slide or be fixed relative to the first segment 14 along the axial direction of the cavity 11, so as to adjust the length of the cavity 11.
[0077] A transparent indicator window can be opened on the shell of the second segment 15, and length markings can be printed on the corresponding positions of the first segment 14 inside. When adjusting, the user can accurately know the length of the current cavity 11 by observing the scale value in the window, thus achieving more precise adjustment.
[0078] The user needs to adjust the length of the device to accommodate different stages of postoperative recovery. Hold the first segment 14 (root segment) and the second segment 15 (front segment) of the device, and then operate the first size adjustment component 5 located between the two segments. Operating the first size adjustment component 5 releases the lock between the second segment 15 and the first segment 14. The user can then smoothly push the second segment 15, allowing it to slide along the outer wall of the first segment 14. When the desired length is reached, the user operates the first size adjustment component 5 to securely fix the second segment 15 in that position, completing the length adjustment.
[0079] The structure of the second segment 15 fitted onto the first segment 14 ensures that the two shell segments remain tightly fitted and coaxially aligned throughout the adjustment process, preventing shaking or misalignment and ensuring the integrity and stability of the structure. Throughout the adjustment process, the cavity 11 remains a continuous cavity composed of the two shell segments, changing only in axial length. This maintains the device's ability to enclose and protect the penis, preventing any gaps that could pinch the skin or leak fluid during adjustment.
[0080] In the specific implementation process, such as Figure 11 , Figures 13-14As shown, the top wall of the first segment 14 has an inner cavity 12 for placing components such as the power supply system. The size of the inner cavity 12 gradually decreases from the side near the first opening 110 to the side near the second opening 111. When the vibration component 3 is installed inside the penile protective cover 1, the vibration component 3 includes a first vibrator 30 installed in the inner cavity 12 of the first segment 14. The first vibrator 30 is installed near the second opening 111. The first vibrator 30 is located in a relatively narrow area within the inner cavity 12, which shortens the transmission path of vibration energy between the first vibrator 30 and the first segment 14 as a whole. The first vibrator 30 can transmit energy to the first segment 14 more directly, reducing energy loss during transmission. Furthermore, the placement of the first vibrator 30 allows more vibration energy to be transmitted to the tip of the penis, allowing more sensitive parts of the penis to receive more vibration energy, making the rehabilitation stimulation effect on the penis more obvious.
[0081] When the vibration component 3 is disposed inside the penile shield 1, the vibration component 3 also includes a second vibrator 31 disposed in the second segment 15, so that the vibration energy of the second vibrator 31 can act more on the front end of the penis, and the intensity of the stimulation applied to the penis by the second vibrator 31 can be adjusted by adjusting the position of the second segment 15.
[0082] One or more flexible sealing rings can be installed at the sliding contact surface between the first section 14 and the second section 15 to prevent external liquids or residual urine from seeping into the device through the gap between the two sections during bathing, thus improving the hygiene level of the product.
[0083] Furthermore, the first size adjustment component 5 includes a slide rail 50 disposed on the first segment 14 and a slider disposed on the second segment 15; like Figures 8-11 As shown, the inner side of the slide 50 is provided with a plurality of positioning grooves 52 along the length of the cavity 11, and the slider is provided with positioning protrusions 53 that are adapted to the positioning grooves 52. When the second segment 15 slides relative to the first segment 14, the positioning protrusions 53 pass through each groove in sequence. When the second segment 15 stops sliding, it is positioned. The protrusions can be engaged with the positioning grooves 52 at the corresponding positions and thus be limited, so that the relative positions of the first segment 14 and the second segment 15 are locked.
[0084] Or, such as Figures 12-14 As shown, a positioning pin 54 and a threaded hole that is adapted to the positioning pin 54 and aligned with the slide rail 50 can be provided on the slider. The positioning pin 54 can be screwed into the slide rail 50 through the threaded hole until it abuts against the bottom wall of the slide rail 50, thereby locking the relative position of the first segment 14 and the second segment 15.
[0085] According to some embodiments of this application, optionally, such as Figure 6 , Figure 15 ,Figure 18 As shown, an elastic positioning ring 112 is provided on the inner side of the cavity 11 surrounding the second opening 111; the positioning ring 112 is used to contact the tip of the penis so that the urethral opening is directly opposite the second opening 111.
[0086] Given that the positioning ring 112 comes into direct contact with sensitive areas of the human body and the environment may be humid, it can be modified with antibacterial materials or treated with a surface coating (such as adding silver ion antibacterial agents). This can effectively inhibit bacterial growth and further improve the hygiene and safety level of the product, which is especially important for postoperative users.
[0087] The cross-section of the positioning ring 112 can be designed as an asymmetrical shape (for example, thicker and softer on the inner side, and thinner and harder on the outer side). This ensures that the inner side, which comes into contact with the skin, is soft and comfortable enough, while also ensuring that the ring has sufficient support strength to stay in the correct position and will not easily shift during wearing or adjustment, thus optimizing the balance between comfort and functionality.
[0088] The positioning ring 112 may be made of, but is not limited to, medical silicone, natural rubber, thermoplastic elastomer (TPE) or foamed polymer.
[0089] When wearing the device, the user inserts the penis into the cavity 11. During insertion, the head of the penis eventually contacts and gently presses against the elastic positioning ring 112 surrounding the inner side of the second opening 111. Because the positioning ring 112 is elastic, it deforms to conform to the shape of the tip of the penis, gently wrapping around and conforming to the contour of the tip. This conformation provides a natural tactile positioning effect. The user can feel that the head of the penis is properly fitted. At this point, thanks to the centered guidance of the positioning ring 112, the user's urethral opening is automatically adjusted to a position directly opposite the second opening 111 of the device.
[0090] The elastic positioning ring 112 achieves rapid and precise positioning of the glans penis within the cavity 11 through physical contact and flexible wrapping. Its core function is to ensure accurate alignment between the urethral opening and the second opening 111. This optimizes urination function, allowing urine to flow directly from the center of the second opening 111, reducing the risk of urine splashing onto the inner wall of the cavity 11 and improving hygiene. Compared to direct contact with the rigid second opening 111, the elastic positioning ring 112 provides soft cushioning, significantly increasing comfort and avoiding pressure and discomfort that may be caused by hard edges, making it especially suitable for sensitive areas after surgery. The deformable properties of the elastic material allow a single positioning ring 112 to adapt to the physiological size differences of different users, ensuring the universality and effectiveness of the positioning function.
[0091] According to some embodiments of this application, optionally, the first size adjustment component 5 is configured to control the second segment 15 to slide until the tip of the penis extends into and is limited by the positioning ring 112, so that the urethral opening is aligned with the second opening 111.
[0092] The term "insertion" as mentioned in this application refers to the tip of the penis entering the space enclosed by the positioning ring 112. The term "limitation" as mentioned in this application is not a completely fixed mechanical jamming, but rather refers to the positioning ring 112 providing a clear, comfortable, and unintentionally difficult final position for the head of the penis through its elastic wrapping force, thereby achieving functional limitation.
[0093] After the user puts on the device, a rough fitting is first performed. Then, the user operates the first size adjustment component 5 to drive the second segment 15 (with the second opening 111 and positioning ring 112) to slide smoothly relative to the first segment 14 along the axial direction. The user adjusts the device while feeling the fit. When adjusted to a certain position, the user will clearly feel the tip of the penis contacting and being gently enveloped by the positioning ring 112, producing a distinct "in place" tactile sensation. At this point, the elastic limiting effect of the positioning ring 112 prevents the head of the penis from moving further forward. This tactile feedback informs the user that the adjustment is complete. Because the positioning ring 112 is precisely positioned around the second opening 111, when the tip of the penis is limited by it, the user's urethral opening is automatically and precisely positioned in the optimal position directly opposite the second opening 111.
[0094] The length adjustment function is linked to the urethral orifice positioning function. Users can reliably achieve the key goal of "urethral orifice aligned with the second opening 111" simply through a simple sliding adjustment and clear tactile feedback, without visual observation or repeated attempts. This simplifies the operation, reduces preparation time for urination, and improves user comfort. The "limiting" function of the positioning ring 112 provides users with a clear and intuitive physical feedback signal (tactile sensation). This makes operation simple and intuitive, improving user experience and operational reliability. Regardless of the user's adjustment, the final stopping position is determined by the interaction between their own physiological structure and the positioning ring 112. This ensures that for a specific user, the unique optimal urethral orifice alignment position is automatically reproduced each time the ring is worn, guaranteeing consistent functional performance.
[0095] According to some embodiments of this application, optionally, such as Figure 15 As shown, the inner surface of the cavity 11 has a flow guiding component 113; the flow guiding component 113 is a flow guiding groove and / or a flow guiding texture.
[0096] A superhydrophobic coating can be applied to an inner surface with drainage grooves or textures. The hydrophobic properties cause the liquid to quickly shrink into a spherical shape, reducing the contact area and adhesion between the liquid and the surface, allowing the droplets to slide and drain at a faster speed under the guidance of the drainage grooves or textures.
[0097] Flow-guiding textures can be microscopic or macroscopic surface raised patterns, such as wave patterns, dot matrix, and diamond-shaped protrusions. These textures can also guide the flow of liquid by disrupting its surface tension and providing direction.
[0098] After a user showers or cleans, numerous tiny water droplets or residual liquid adhere to the inner surface of the cavity 11. Due to the flow-guiding components 113 on the inner surface, these dispersed droplets do not scatter randomly. Under the combined influence of gravity, vibration, and liquid surface tension, the liquid naturally flows along the path planned by these pre-designed flow-guiding grooves or textures. These grooves and textures collect the dispersed liquid and guide it towards the bottom of the cavity 11 (i.e., the end near the second opening 111). Finally, the collected liquid is discharged from the second opening 111 and the opening of the mesh structure, thus achieving rapid drying of the interior of the cavity 11.
[0099] The flow guiding component 113 actively provides a flow path for the liquid, overcoming the problem of liquid spreading and adhering easily on flat or simple curved surfaces, transforming disordered droplets into orderly flow, and accelerating the speed and efficiency of liquid discharge. By guiding residual liquid from various parts of the cavity to the outlet for centralized discharge, the flow guiding component 113 reduces the difficulty of drying in certain areas due to liquid retention, achieving more comprehensive and faster drying inside the cavity 11, and improving the hygiene level of use.
[0100] In practice, differentiated flow guidance schemes can be designed based on the characteristics of different areas within the cavity 11. For example, sparse, shallow, and wide flow guidance channels are used on the upper sidewall of the cavity 11 for initial flow collection; while denser and deeper flow guidance channels are used near the bottom for rapid drainage and final discharge. This zoning design allows for more precise and efficient management of the entire liquid collection and discharge process.
[0101] According to some embodiments of this application, optionally, such as Figure 16 As shown, the outer surface of the penis shield 1 is provided with a draining section 13; the flow guiding component 113 is configured to guide the liquid in the cavity 11 to the draining section 13.
[0102] The flow channels or textures (i.e., the flow guide assembly 113) guide the liquid remaining on the inner wall of the cavity 11 to the second opening 111 and the opening of the mesh structure at the bottom. After the liquid is discharged, it flows onto the draining portion 13 located on the outer surface of the penile shield 1, immediately below the second opening 111. The special geometry of the draining portion 13 (such as a downwardly convex curved surface) further gathers the outflowing liquid, causing it to aggregate into larger droplets. When the droplet is heavy enough, it drips from the tip of the draining portion 13, thus completely detaching from the device.
[0103] The flow guiding component 113 inside the cavity 11 ensures that the liquid can be quickly collected and discharged from the cavity, while the externally located draining part 13 ensures that the discharged liquid is effectively treated without wetting the user. The two work together to accelerate the overall drying process and improve hygiene.
[0104] According to some embodiments of this application, optionally, a vibration control program is also included for driving the vibration assembly 3 to perform water removal vibration and automatically stopping after a rated time is reached.
[0105] After showering or cleaning, the user needs to remove the water from the cavity 11. They do not need to continuously press and hold the switch on the vibration component 3; they simply need to trigger a "water removal" command once via a button on the device or a remote control (such as a remote control or app). This command activates the built-in vibration control program. The program then drives the vibration component 3 to start working in a specific mode (i.e., water removal vibration). Without any further user intervention, the program will automatically stop the vibration component 3 after running for a pre-set time.
[0106] The vibration control program encapsulates the water removal function into a one-button triggered automated process, greatly simplifying the user experience by eliminating the need for complex operations or timing. The automatic stop mechanism after the rated time prevents the vibration component 3 from running idle for extended periods due to user forgetting to turn it off, effectively saving battery power and preventing potential lifespan reduction due to motor overheating or prolonged operation. The wearable protective massage device provided in this application uses a vibration control program to solidify the water removal process, ensuring consistent and reliable water removal results each time, avoiding differences in effectiveness caused by varying user manual operation times.
[0107] According to some embodiments of this application, optionally, water removal vibration refers to the vibration component 3 alternating between a vibration state and a stop state to achieve effective collection and discharge of liquid.
[0108] The vibration period and the stop period of the vibrating component 3 can be equal or unequal (for example, vibrating for 0.2 to 1 second and stopping for 1 to 2 seconds). The core principle is the existence of a working cycle that is repeated. The specific duty cycle can be determined experimentally based on the optimal water removal effect.
[0109] During the vibration phase, droplet desorption occurs; during the stationary phase, droplet confluence and guidance occur. Alternating between these two sub-processes is more effective than simply continuing vibration to complete only the first process.
[0110] After the user activates the dewatering function, the vibration control program begins to operate. Instead of continuously running the motor, it executes a vibration-pause-vibration cycle. For example, the program first drives the vibration component 3 to vibrate strongly for one second. This short, powerful vibration effectively shakes water droplets adhering to the inner wall of the cavity 11 off the surface. Then, the program controls the vibration to stop, entering a 1.5-second pause. During this static period, the water droplets that have just been shaken off flow naturally downwards along the inner wall or the guide component 113 under the influence of gravity, converging. Then, the next vibration cycle begins, shaking off any small or medium-sized droplets that failed to flow away on their own, and propelling the already converged droplets towards the second opening 111 and the bottom mesh structure opening. This cycle repeats several times until the total predetermined time is reached, at which point it automatically stops.
[0111] This combination of dynamic and static vibration is more efficient than continuous vibration. The vibrating state shakes the liquid off the surface, while the stationary state provides the necessary settling time for the liquid to flow and collect naturally under gravity. This alternation simulates the optimal physical process of slapping and flowing, resulting in faster and more thorough liquid removal. Intermittent operation means the total motor runtime is significantly shorter than with continuous vibration, significantly reducing energy consumption and extending battery life, meeting the energy-saving requirements of wearable devices. The short, intermittent vibration avoids the numbness or discomfort that prolonged continuous vibration might cause to sensitive areas, improving the user experience.
[0112] According to some embodiments of this application, optionally, a key is also included, which is used to unlock the locking state between the first locking part 10 and the second locking part 20.
[0113] The presence of a key prevents the device from being arbitrarily opened, ensuring its stability and tamper-proof nature during wear. This is particularly useful in medical settings, preventing patients from prematurely removing the device due to discomfort, which could affect postoperative recovery, and enabling authorized management controlled by nursing staff. The reliable mechanical locking structure avoids the risk of accidental opening due to impacts or snagging in daily life, enhancing safety. Furthermore, for users who need to wear the device long-term, this design, which allows unauthorized opening, provides a sense of security. The purely mechanical key unlocking method does not rely on electricity, signals, or complex procedures, ensuring immediate and reliable operation in any environment (such as a damp bathroom), guaranteeing absolute functionality.
[0114] In practical implementation, in extreme situations (such as lost keys or sudden medical emergencies requiring urgent medical attention), a keyless emergency unlocking method can be implemented. For example, a mechanical lock with a fracture-resistant weakening structure can be used. When a specific, large abnormal force is applied, this structure will break, thereby achieving emergency unlocking. This ensures both daily reliability and safety redundancy in extreme situations. According to some embodiments of this application, optionally, such as Figures 17-19 As shown, the second locking part 20 is configured to adjust its locking position with the first locking part 10 in order to adjust the diameter of the closed slit 4 accordingly.
[0115] By adjusting the locking position, users can precisely adjust the actual diameter of the closed slit 4 according to their own physiological structure and comfort perception. This solves the common problem of discomfort due to excessive tightness or easy slippage due to excessive looseness caused by individual differences, achieving personalized customization and improving the user experience.
[0116] In practice, the second locking part 20 of the testicular locking assembly 2 can be equipped with clear scale markings or raised dots with different tactile sensations. This helps users quantify the adjustment range and record the most suitable position for themselves, making it easy to quickly return to the optimal state the next time they wear it, without having to try repeatedly.
[0117] A soft, elastic pad can be integrated into the inside of the testicular locking assembly 2 (the side that contacts the skin). Even if the user adjusts the lock slightly tighter, the elastic pad can cushion the pressure and distribute the pressure through its own deformation, further improving comfort while ensuring the anti-slip effect.
[0118] Although this application has been described with reference to preferred embodiments, various modifications can be made thereto and components can be replaced with equivalents without departing from the scope of this application. In particular, the technical features mentioned in the various embodiments can be combined in any manner, provided there is no structural conflict. This application is not limited to the specific embodiments disclosed herein, but includes all technical solutions falling within the scope of the claims.
Claims
1. A wearable protective massage device, characterized in that, include: The penis shield is equipped with a first locking part; The testicular locking assembly is provided with a second locking part; Vibration components; The penile shield is formed by a shell with a mesh or partially mesh structure, and its interior forms a cavity for accommodating the penis. The first locking part and the second locking part are locked together in an unlockable manner; When the first locking part and the second locking part are in the locking state, a closed narrow slit is formed between the testicular locking assembly and the penile protective shield. The closed narrow slit is used to clamp the base of the scrotum, and the size of the closed narrow slit is configured to prevent the scrotum from slipping off. The vibration component is located inside the penile shield and / or connected to the penile shield.
2. The wearable protective massage device according to claim 1, characterized in that, Also includes: Remote control terminal; A wireless control component, comprising a first communication unit and a second communication unit; The vibration assembly has a drive control terminal; The first communication unit and the second communication unit are respectively located at the remote control terminal and the drive control terminal, and are used to transmit control signals from the remote control terminal.
3. A wearable protective massage device according to claim 1 or 2, characterized in that, The cavity has a first opening and a second opening; The cavity is a long strip-shaped structure with an approximately circular cross-section that extends perpendicularly to its length direction; Wherein, the first opening and the second opening are located at both ends of the length direction of the cavity; Wherein, the length direction of the cavity is the axial direction of the elongated shape of the cavity; The first locking part is located at the first opening.
4. A wearable protective massage device according to claim 3, characterized in that, The diameter of the second opening is 1 / 5 to 1 / 2 of the diameter of the first opening.
5. A wearable protective massage device according to claim 4, characterized in that, The penis shield is provided with a drip-collecting section near the second opening; The draining section is configured to collect surrounding liquid and form droplets when the user wears it standing up, and to cause the droplets to fall.
6. A wearable protective massage device according to claim 3, characterized in that, Also includes: A first size adjustment component is used to adjust the length of the cavity.
7. A wearable protective massage device according to claim 6, characterized in that, The penile shield includes a first section and a second section arranged sequentially along the axial direction of the cavity; The first opening is located in the first segment, and the second opening is located in the second segment; The second segment is fitted over the first segment, and the first size adjustment component is disposed between the first segment and the second segment; The first size adjustment component is used to control the second segment to slide or be fixed relative to the first segment along the axial direction of the cavity, so as to adjust the length of the cavity.
8. A wearable protective massage device according to claim 7, characterized in that, An elastic positioning ring is provided around the second opening on the inner side of the cavity; The positioning ring is used to contact the tip of the penis so that the urethral opening is aligned with the second opening.
9. A wearable protective massage device according to claim 8, characterized in that, The first size adjustment component is configured to control the second segment to slide until the tip of the penis extends into and is limited by the positioning ring, so that the urethral opening is aligned with the second opening.
10. A wearable protective massage device according to any one of claims 1 to 6, characterized in that, The inner surface of the cavity has a flow guiding component; The flow guiding component is a flow guiding groove and / or a flow guiding texture.
11. A wearable protective massage device according to claim 10, characterized in that, The outer surface of the penis shield is provided with a drip collection section; The flow guiding component is configured to guide the liquid in the cavity to the confluence dripping section.
12. A wearable protective massage device according to claim 1, characterized in that, Also includes: A vibration control program is used to drive the vibration assembly to perform water removal vibration and automatically stop after a rated time.
13. A wearable protective massage device according to claim 12, characterized in that, The water removal vibration refers to the alternating switching of the vibration component between a vibration state and a stop state to achieve effective collection and discharge of liquid.
14. A wearable protective massage device according to claim 1, characterized in that, Also includes: A key is used to unlock the locking state between the first locking part and the second locking part.
15. A wearable protective massage device according to claim 1, characterized in that, The second locking part is configured to adjust its locking position with the first locking part to adjust the diameter of the closed slit accordingly.