Snore treatment instrument

Abstract

The snore treatment instrument comprises a shell, an isolation plate and a vibration unit, the shell is provided with an inner cavity, an air inlet end and an air outlet end, and the air inlet end and the air outlet end communicate with the inner cavity; the isolation plate is arranged in the shell and divides the inner cavity into a first cavity and a second cavity, and the isolation plate is provided with an opening; the vibration unit comprises a support, a swing arm and a switch valve, the support comprises a base and a rotating shaft, the base is fixed to the isolation plate, the first end of the swing arm is close to the air inlet end and rotatably connected with the base through the rotating shaft, the second end of the swing arm is close to the air outlet end and is a free end, and the switch valve is connected with the first end and the second end. The opening is sealed by the switch valve in a natural state, and the switch valve can rotate around the rotating shaft along with the swing arm under blowing of expiration airflow so that the expiration airflow can flow into the second cavity through the opening and flow out of the air outlet end. According to the snore treatment instrument, the number of the rotating shaft is one, the whole rotating shaft penetrates through the base and the swing arm, and the matching precision of the snore treatment instrument is improved.

Description

Technical Field

[0001] This application relates to the field of fitness equipment technology, and more particularly to an anti-snoring device. Background Technology

[0002] Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS, OSAS) is a condition characterized by sleep apnea caused by obstructive lesions of the upper airway (including collapse of the pharyngeal mucosa), and is mainly manifested as snoring during sleep.

[0003] Upper airway muscle weakness is a common cause of obstructive snoring syndrome (OSAS). Weak, thickened, and crowded neck and pharyngeal muscles can easily lead to upper airway obstruction. Treatment methods for snoring generally include surgical removal, anti-snoring devices, and exercise-based weight loss therapies.

[0004] Surgical resection is an invasive procedure that involves removing parts of the upper airway that are significantly narrowed due to enlarged tonsils or adenoids. It is a traumatic intervention that is difficult for users to accept.

[0005] Anti-snoring therapy is currently the main method for preventing snoring during sleep. This involves using a CPAP machine, anti-snoring patches, mouthguards, or belts before bed to keep the airway clear during sleep. However, because these devices need to be worn constantly during sleep, user acceptance is low, and users tend to resume snoring once the device is removed. Therefore, anti-snoring therapy only addresses the symptoms, not the root cause; it can only stop snoring, not cure it.

[0006] Exercise therapy can fundamentally solve the problem of respiratory muscle weakness caused by obesity. However, exercise requires a certain space and time. Nowadays, most people are too busy to find the time and suitable place to exercise for weight loss. Moreover, the effects of exercise are mainly reflected on the surface of the body and cannot directly exercise the throat and pharynx inside the cavity.

[0007] Some existing fitness equipment involving respiratory management has many internal structures in order to achieve better therapeutic effects, but the coordination between the structures is often low and the vibration effect is poor, which greatly affects the fitness effect. Utility Model Content

[0008] This application proposes an anti-snoring device to improve the fitting accuracy of the anti-snoring device.

[0009] The embodiments of this application achieve the above objectives through the following technical solutions.

[0010] An anti-snoring device includes a housing, an isolation plate, and a vibration unit. The housing has an inner cavity, an air inlet, and an air outlet communicating with the inner cavity. The isolation plate is disposed inside the housing, dividing the inner cavity into a first cavity and a second cavity, and the isolation plate has an opening. The vibration unit includes a support, a swing arm, and a switching valve. The support includes a base and a rotating shaft. The base is fixed to the isolation plate. The first end of the swing arm is close to the air inlet and rotatably connected to the base via the rotating shaft. The second end of the swing arm is close to the air outlet and is a free end. The switching valve connects the first end and the second end. In its natural state, the switching valve closes the opening and can rotate around the rotating shaft with the swing arm under the blowing of the expiratory airflow, allowing the expiratory airflow to flow into the second cavity through the opening and out from the air outlet.

[0011] In one embodiment, the clearance fit between the rotating shaft and the swing arm is 0.2mm to 0.5mm.

[0012] In one embodiment, the swing arm is provided with a first through hole and a second through hole, and the rotating shaft passes through the first through hole and the second through hole. The clearance fit between the rotating shaft and the first through hole is 0.2mm to 0.5mm, and the clearance fit between the rotating shaft and the second through hole is 0.2mm to 0.5mm.

[0013] In one embodiment, the partition plate includes a substrate and a frustum-shaped extension extending from the substrate toward a first cavity, with an opening penetrating the extension.

[0014] In one embodiment, the circumferential surface of the extension is an arc surface, and the contact point between the switch valve and the arc surface forms a closed curve.

[0015] In one embodiment, the switching valve is conical with a rounded apex and a radius of 0.1cm to 0.9cm.

[0016] In one embodiment, the anti-snoring device further includes a first magnetic unit and a second magnetic unit. The first magnetic unit is disposed at the second end of the swing arm, and the second magnetic unit is disposed on the inner wall of the housing. The second magnetic unit is used to attract the first magnetic unit so that the swing arm can return to the closed opening of the switch valve along with the switch valve when there is a lack of expiratory airflow.

[0017] In one implementation, the switching valve and the rocker arm are connected by a flexible connection.

[0018] In one implementation, the power arm and resistance arm of the swing arm are of equal length.

[0019] In one implementation, the power arm of the swing arm is longer than the resistance arm.

[0020] Compared to existing technologies, the anti-snoring device provided in this application has a single rotating shaft that runs through the base and the swing arm, resulting in high overall precision. This prevents the vibration unit from jamming or becoming unbalanced during swinging due to precision issues, thus greatly improving the treatment effect. Attached Figure Description

[0021] To more clearly illustrate the technical solutions in the embodiments of this application, the accompanying drawings used in the description of the embodiments will be briefly introduced below. Obviously, the accompanying drawings described below are only some embodiments of this application. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0022] Figure 1 This is a schematic diagram of the anti-snoring device provided in the embodiments of this application (excluding the rotating shaft);

[0023] Figure 2 yes Figure 1 The diagram shows the structure of the isolation plate and vibration unit of the anti-snoring device.

[0024] Figure 3 This is a longitudinal cross-sectional schematic diagram of the anti-snoring device provided in the embodiments of this application;

[0025] Figure 4 This is a schematic diagram showing the cooperation relationship between the switching valve and the opening of the anti-snoring device provided in the embodiments of this application;

[0026] Figure 5 This is a schematic diagram showing the length relationship between the power arm M1 and the resistance arm R1 of the vibration unit of the anti-snoring device provided in this application embodiment. Detailed Implementation

[0027] To enable those skilled in the art to better understand the present application, the technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are merely some embodiments of the present application, and not all embodiments. Furthermore, all other embodiments obtained by those skilled in the art based on the embodiments of the present application without creative effort are within the scope of protection of the present application.

[0028] It should be noted that all directional indications in the embodiments of this application are only used to explain the relative positional relationship and movement of each component in a specific posture. If the specific posture changes, the directional indications will also change accordingly.

[0029] Furthermore, the technical solutions of the various embodiments of this application can be combined with each other, but only if they are based on the ability of those skilled in the art to implement them. When the combination of technical solutions is contradictory or cannot be implemented, it should be considered that such combination of technical solutions does not exist and is not within the scope of protection claimed by this application.

[0030] Unless otherwise specified, the "natural state" mentioned in this application refers to the state when the anti-snoring device is placed on a horizontal plane and there is no exhaled airflow. "Frustum" refers to the portion between the base of a cone and the cross-section when a cone is cut by a plane parallel to its base.

[0031] Please see Figure 1 , Figure 2 and Figure 3 This application provides an anti-snoring device 1, including a housing 10, an isolation plate 12, and a vibration unit 14. The housing 10 has an inner cavity 100, and the housing 10 also has an air inlet and an air outlet communicating with the inner cavity 100; the isolation plate 12 is disposed inside the housing 10 and isolates the inner cavity 100 into a first cavity 1001 and a second cavity 1002, and the isolation plate 12 is provided with an opening 120. The vibration unit 14 includes a bracket 141, a swing arm 142, and a switching valve 143. The bracket 141 includes a base 1412 and a rotating shaft 1414. The base 1412 is fixed to the isolation plate 12. The first end 1421 of the swing arm 142 is close to the air inlet and is rotatably connected to the base 1412 through the rotating shaft 1414. The second end 1422 of the swing arm 142 is close to the air outlet and is a free end. The switching valve 143 seals the opening 120 in its natural state and can rotate with the swing arm 142 around the rotating shaft 1414 under the blowing of the exhaled airflow, so that the exhaled airflow can flow into the second chamber 1002 through the opening 120 and flow out from the air outlet.

[0032] The bracket 141 of the vibration unit 14 fixes the isolation plate 12. The bracket 141 supports the swing arm 142 and also serves as the fulcrum of the swing arm 142. The bracket 141 and the isolation plate 12 can be integrally formed or fixedly connected to each other. When the bracket 141 and the isolation plate 12 are integrally formed, the structural precision of the anti-snoring device 1 is higher.

[0033] Since there is only one rotating shaft 1414, which runs through the base 1412 and the swing arm 142, the swing arm 142 can rotate around the rotating shaft 1414 very accurately. Compared with the technical solution of setting a rotating shaft on each side of the swing arm 142, the rotation of the swing arm 142 is smooth and can maintain balance well.

[0034] In addition to improving the overall fit of the vibration unit 14 and preventing the vibration unit 14 from jamming or becoming unbalanced during swinging, the width of the swing arm 142 can be set to be relatively smaller since there is no need to set rotation shafts on both sides of the swing arm 142, thus optimizing the product structure.

[0035] In some embodiments, the rotating shaft 1414 and the base 1412 are fixedly arranged relative to each other, for example, by welding, gluing or other means, to fix the rotating shaft 1414 relative to the base 1412.

[0036] In this embodiment, the base 1412 includes a first sub-base 14125 and a second sub-base 14126, which are arranged opposite to each other. The first sub-base 14125 is provided with a first connecting hole 14121, and the second sub-base 14126 is provided with a second connecting hole 14122. The first connecting hole 14121 and the second connecting hole 14122 are coaxial, and the rotating shaft 1414 passes through the first connecting hole 14121 and the second connecting hole 14122.

[0037] The rotating shaft 1414 also passes through the swing arm 142, allowing the swing arm 142 to rotate relative to the rotating shaft 142. Specifically, the swing arm 142 is provided with a first through hole 1423 and a second through hole 1424, and the rotating shaft 1414 passes through the first through hole 1423 and the second through hole 1424. In some embodiments, the clearance fit between the rotating shaft 1414 and the first through hole 1423 is 0.2mm to 0.5mm, and the clearance fit between the rotating shaft 1414 and the second through hole 1424 is 0.2mm to 0.5mm. This clearance fit allows the vibration unit 14 some room for movement. During the reset process of the vibration unit 14, when there is a slight misalignment between the switch valve 143 and the opening 120, this extra room for movement can give the switch valve 143 the ability to automatically align, resulting in better sealing between the switch valve 143 and the opening 120.

[0038] The housing 10 of the anti-snoring device 1 is roughly a hollow cylindrical structure, with the hollow area forming an inner cavity 100. On the left side of the diagram is the air inlet of the anti-snoring device 1, and on the right side is the air outlet. The air inlet and outlet do not refer to any specific structure, but merely indicate direction.

[0039] In addition to the walls forming the external structure, the housing 10 also includes several supporting walls or structural walls in the inner cavity 100. For example, the housing 10 also includes a radial sidewall 1010 and a bottom wall 1012 perpendicular to the inner surface of the housing 10, with the bottom wall 1012 near the air outlet. The radial sidewall 1010 partially blocks the air inlet along the radial direction of the anti-snoring device 1, guiding the expiratory airflow to the lower part of the anti-snoring device 1 and reducing the air inlet cross-sectional area. The partition plate 12 is a thin plate-like structure connected between the radial sidewall 1010 and the bottom wall 1012, thereby dividing the inner cavity 100 into two stacked chambers, namely the first chamber 1001 and the second chamber 1002. The first chamber 1001 is at the bottom, and the second chamber 1002 is at the top. The expiratory airflow enters the first chamber 1001 from the air inlet, then enters the second chamber 1002 through the opening 120, and then exits from the air outlet on the right side. The bottom wall 1012 can also be a section of wall extending outward from the partition plate 12.

[0040] In some embodiments, the housing 10 includes a first outer side wall 191 and a second outer side wall 192, which are connected to each other to form a cylinder with an inner cavity 100.

[0041] In other embodiments, the housing 10 may also be a one-piece structure, as long as it can be divided into two interconnected cavities inside.

[0042] In some embodiments, the partition plate 12 and the housing 10 are integrally formed. In some embodiments, the partition plate 12 is fixedly connected to the housing 10, for example, by welding, snap-fit ​​connection, etc.

[0043] The partition plate 12 has an opening 120, the axis of which is perpendicular or substantially perpendicular to the partition plate 120. In some embodiments, the height of the opening 120 may be equal to the thickness of the partition plate 12. In this embodiment, the opening 120 is conical, and the conical shape is more conducive to guiding the airflow of the first chamber 1001 into the second chamber 1002.

[0044] The isolation plate 12 includes a base plate 124 and a frustum-shaped extension 126. The extension 126 extends from the base plate 124 toward the first cavity 1001, and an opening 120 passes through the extension 126. The central axis of the opening 120 is perpendicular to the base plate 124.

[0045] The substrate 124 can be a plate-like structure, including an upper surface 1241 and a lower surface 1242 facing away from each other. At the location where the opening 120 is required, the upper surface 1241 and lower surface 1242 extend outward from the plane containing the substrate 124 to form an extension 126. The upper surface 1241 and lower surface 1242 can be bent into an arc shape, and the thickness of the extension 126 is the same as the thickness of the substrate 124. Forming the opening 120 directly on the isolation plate 12 simplifies the internal structure compared to adding an additional structure for placing the switching valve to the isolation plate 12, reduces assembly errors between other structures and the isolation plate, improves the fitting accuracy between structures, and ensures a sealing effect.

[0046] In this embodiment, the extension 126 extends relative to the substrate 124 into the first cavity 1001, eliminating the need to reserve space for the extension 126 separately. This reduces the overall height of the anti-snoring device 1 in the axial direction of the opening 120, further reducing the product volume in that direction and making the product more compact and practical.

[0047] The swing arm 142 is a narrow and long plate, which is arranged along the length of the air inlet and the air outlet. The swing arm 142 includes a first end 1421 and a second end 1422, which are opposite each other. The first end 1421 is close to the air inlet and the second end 1422 is close to the air outlet.

[0048] The switching valve 143 is disposed near the second end 1422. The shape of the switching valve 143 matches the shape of the opening 120, as long as it can seal the opening 120. In this embodiment, the circumferential surface of the extension 126 is an arc surface, and the opening 120 is a roughly truncated cone. The switching valve 143 includes a tapered portion 1432 extending away from the swing arm 142 to contact the circumferential surface of the extension 126. All contact points form a closed curve S (see [reference]). Figure 4 This not only effectively seals the opening 120, but also minimizes the contact area, greatly reducing friction between the two, allowing the switch valve 143 to be opened with minimal exhalation. In other embodiments, the switch valve 143 and the opening 120 can also be a surface fit, meaning the contact area has a certain area.

[0049] In one embodiment, the switching valve 143 is conical, with a rounded apex and a radius of 0.1 cm to 0.9 cm. Since the switching valve 143 needs to quickly return to its original state after being subjected to a rebound force, the lower the resistance during the reset process, the better; therefore, a smaller apex is preferable, as this reduces rebound resistance. In other embodiments, the switching valve 143 can also be spherical or other shapes suitable for mating with the opening 120.

[0050] When no expiratory airflow passes through opening 120, the vibrating unit 14 is in its natural state, and the switching valve 143 blocks opening 120. When expiratory airflow passes through opening 120, the switching valve 143 is opened by the expiratory airflow, causing the swing arm 142 to swing, creating a gap between the switching valve 143 and opening 120, allowing expiratory airflow to enter the second chamber 1002. As the force of the expiratory airflow on the switching valve 143 gradually decreases, the switching valve 143 falls back to its original position, sealing opening 120, and the vibrating unit 14 stops swinging. When expiratory airflow continuously enters the first chamber 1001, the vibrating unit 14 will continuously swing, generating vibrational sound waves and causing vibration of the upper respiratory tract muscles.

[0051] The vibration unit 14 can be made of polymer materials commonly used in medical applications, such as polycarbonate (PC), which has good biocompatibility and a simple and stable structure.

[0052] Please see Figure 4 and Figure 5In this embodiment, the swing arm 142 is divided into two sections by the bracket 141. Since the switching valve 143 is located in the section near the outlet end, this section is lifted by the exhaled airflow, and therefore this section has a power arm M1. Correspondingly, the section near the inlet end has a resistance arm R1. In this embodiment, the power arm M1 is longer than the resistance arm R1. In other embodiments, the power arm M1 and the resistance arm R1 can be equal or substantially equal. When the power arm M1 is longer than the resistance arm R1, it can promote faster reset of the end of the resistance arm R1 and shorten the length of the swing arm 142 on the side of the resistance arm R1, reducing the product size and making it easier to carry, allowing users to perform treatment and exercise anytime and anywhere.

[0053] Please refer to the following: Figure 3 In some embodiments, the switching valve 143 and the rocker arm 1412 are connected by a flexible connection. The switching valve 143 is located on the side of the rocker arm 142 near the second end 1422 and forms a flexible connection with the rocker arm 142. That is, it is connected by a flexible material or a spring structure 150. In this way, the switching valve 143 can undergo slight deformation when subjected to external force. During the reset process of the vibration unit 14, if the switching valve 143 and the opening 120 are slightly misaligned, under the reset inertia of the switching valve 143 and the interaction between the switching valve 143 and the opening 120, this slight deformation caused by the flexible connection allows the switching valve 143 to automatically align with the opening 120, thereby achieving a precise seal.

[0054] In some embodiments, the anti-snoring device 1 further includes a first magnetic unit 161 and a second magnetic unit 162. The first magnetic unit 161 is disposed on the swing arm 142, and the second magnetic unit 162 is disposed on the inner wall of the housing 10. The second magnetic unit 162 is used to attract the first magnetic unit 161 so that the swing arm 142 can be reset to the closed opening 120 of the switch valve 143 along with the switch valve 143 when there is a lack of expiratory airflow.

[0055] The first magnetic unit 161 can rotate together with the swing arm 142. The first magnetic unit 161 can be set in a specially opened mounting slot in the swing arm 142, or it can be directly set on the surface of the swing arm 142.

[0056] The second magnetic unit 162 is disposed on the housing 10. It can be disposed on the inner surface of the housing 10 facing the inner cavity 100, on the bottom wall 1012, or even on the outer surface of the housing 10. In short, it can be disposed in a position that can attract the swing arm 142 to reset. In this embodiment, the second magnetic unit 162 is located in the second cavity 1002, near the air outlet end.

[0057] The advantage of this design is that during the reset process of the vibration unit 14, the attraction between the first magnetic unit 161 and the second magnetic unit 162 helps the vibration unit 14 to reset normally even after being subjected to air intake force or other forces. This allows the user to use the anti-snoring device 1 without being affected by their posture, enabling them to exercise anytime, anywhere, in any position. For example, when the user needs to lie on their side due to physical reasons, the reset direction of the switch valve 143 will form an acute or obtuse angle with the direction of gravity of the anti-snoring device 1. Especially when it forms an obtuse angle, the direction of the component of gravity is opposite to the reset direction of the switch valve 143, which will hinder the reset of the switch valve 143. However, since there is always a component of the force between the first magnetic unit 161 and the second magnetic unit 162 that is consistent with the reset direction of the switch valve 143, the switch valve 143 can reset in any usage posture, thus achieving the goal of allowing the user to use the anti-snoring device 1 in any posture.

[0058] When the frequency range of the vibration sound wave is 20 to 200 Hz, the anti-snoring device provided in this application embodiment can accurately exercise the muscles of the upper respiratory tract, strengthen the muscles of the upper respiratory tract, prevent the muscles from relaxing and sagging after sleep, and block the upper respiratory tract, thereby achieving the purpose of treating snoring.

[0059] In some embodiments, when the frequency range of the vibration sound wave is 20 to 110 Hz, it can more accurately exercise the muscles of the upper respiratory tract and better achieve the purpose of treating snoring.

[0060] The frequency of the vibration waves can be adjusted adaptively for different stages of use. As the training progresses, the muscles of the upper respiratory tract become stronger, and the required vibration frequency also changes. For example, in the early stages of training, when the muscles are relatively relaxed, a vibration frequency of 20-75Hz is sufficient. In later stages, as the upper respiratory tract muscles have developed a certain strength, the vibration caused by the original vibration frequency becomes weaker. Therefore, by adjusting the frequency or changing to different anti-snoring devices, a vibration frequency of 65-110Hz can be used to increase the intensity of later training and ensure the continued stability of the treatment effect.

[0061] Regardless of the stage, the vibration frequency of the anti-snoring device provided in this application embodiment can be tested in the following ways, and the testing methods may include, but are not limited to, at least one of the following methods:

[0062] 1. When the detection device is a power source type, use instruments such as a ventilator to output a fixed air pressure of 15-100 cmH2O and a flow rate of 25-70 L / min to the shell of the anti-snoring device, for example, to the vibration unit, and measure the vibration frequency of the vibration unit using instruments such as a laser vibrometer and a sound wave detector.

[0063] 2. Through clinical use, healthy individuals over 15 years of age should take a deep breath and forcefully exhale onto the shell of the anti-snoring device. The vibration frequency of the vibration unit should be measured using instruments such as a laser vibrometer and a sound wave detector.

[0064] 3. The vibration frequency was obtained by applying boundary conditions of 15-100 cm water column (cmH2O) air pressure and 25-70 L / min to the shell of the anti-snoring device through computational simulation.

[0065] Through continuous testing and adjustments to the structure of the vibration unit or the entire anti-snoring device, the vibration frequency of the vibration unit is made to fall within the frequency range required by this application. This frequency testing and adjustment method is not limited to the anti-snoring device provided in the embodiments of this application.

[0066] The above embodiments are only used to illustrate the technical solutions of this application, and are not intended to limit them. Although this application has been described in detail with reference to the foregoing embodiments, those skilled in the art should understand that modifications can still be made to the technical solutions described in the foregoing embodiments, or equivalent substitutions can be made to some of the technical features. Such modifications or substitutions do not cause the essence of the corresponding technical solutions to deviate from the spirit and scope of the technical solutions of the embodiments of this application, and should all be included within the protection scope of this application.

Claims

1. An anti-snoring device, characterized in that, The application relates to a snore treatment device. The device comprises a housing with an inner cavity, an air inlet and an air outlet; a partition plate arranged in the housing to divide the inner cavity into a first cavity and a second cavity, the partition plate being provided with an opening; and a vibration unit comprising a support, a swing arm and a switch valve, the support comprising a base and a rotating shaft, the base being fixed to the partition plate, a first end of the swing arm being rotatably connected to the base via the rotating shaft, a second end of the swing arm being close to the air outlet and being a free end, the switch valve being connected to the first end and the second end, the switch valve being closed to the opening in a natural state and being capable of rotating with the swing arm around the rotating shaft under the blowing of exhalation airflow so that the exhalation airflow can flow into the second cavity through the opening and flow out of the air outlet. The gap between the rotating shaft and the swing arm is 0.2-0.5 mm. The swing arm is provided with a first through hole and a second through hole, the rotating shaft penetrating the first through hole and the second through hole, the gap between the rotating shaft and the first through hole being 0.2-0.5 mm, and the gap between the rotating shaft and the second through hole being 0.2-0.5 mm. The partition plate comprises a base plate and an extension in the shape of a circular truncated cone, the extension extending from the base plate to the first cavity, and the opening penetrating the extension.

2. The snore treatment appliance of claim 1, wherein The peripheral surface of the extension is a circular arc surface, and the contact points of the switch valve and the circular arc surface are connected to form a closed curve.

3. The snore treatment appliance of claim 2, wherein, The switch valve is in the shape of a circular cone, the top angle of the circular cone being a rounded angle, and the radius of the rounded angle being 0.1-0.9 cm.

4. The snore treatment appliance of claim 1, wherein, The snore treatment device further comprises a first magnetic unit arranged at the second end of the swing arm and a second magnetic unit arranged on the inner wall of the housing, the first magnetic unit being attracted by the second magnetic unit so that the swing arm can be reset with the switch valve to close the opening in the absence of blowing of exhalation airflow.

5. The snore treatment appliance of claim 4, wherein, The swing arm and the switch valve are connected by a soft connection.

6. The snore treatment appliance of claim 1, wherein, The power arm and the resistance arm of the swing arm are equal in length.

7. The snore treatment appliance of claim 1, wherein The power arm of the swing arm is longer than the resistance arm.

8. The snore treatment appliance of claim 1, wherein, ​ 9. The snore treatment appliance of claim 1, wherein, ​ 10. The snore treatment appliance of claim 1, wherein, ​

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