62 results about "Implant surgery" patented technology

Systems and methods for providing assistance to a surgeon during an implant surgery are disclosed. A method includes defining areas of interest in diagnostic data of a patient and defining a screw bone type based on the surgeon's input. Post defining the areas of interest, salient points are determined for the areas of interest. Successively, an XZ angle, an XY angle, and a position entry point for a screw are determined based on the salient points of the areas of interest. Successively, a maximum screw diameter and a length of the screw are determined based on the salient points. Thereafter, the screw is identified and suggested to the surgeon for usage during the implant surgery.

Systems and methods for providing assistance to a surgeon during an implant surgery are disclosed. A method includes defining areas of interest in diagnostic data of a patient and defining a screw bone type based on the surgeon's input. Post defining the areas of interest, salient points are determined for the areas of interest. Successively, an XZ angle, an XY angle, and a position entry point for a screw are determined based on the salient points of the areas of interest. Successively, a maximum screw diameter and a length of the screw are determined based on the salient points. Thereafter, the screw is identified and suggested to the surgeon for usage during the implant surgery.

The utility model provides a sheet-shaped electrode and an implantation device, the sheet-shaped electrode comprises an electrode slice, the surface of the electrode slice is provided with an electrode contact, the electrode slice has flexibility, and the electrode slice can be curled and contracted into a cylindrical shape matched with a pushing catheter, or the electrode slice can be unfolded into a sheet shape outside the pushing catheter; and the electrode wire is connected to one end of the electrode plate, the electrode wire is electrically connected with the electrode contact, the electrode wire can be arranged in the pushing catheter or the withdrawing catheter in a penetrating manner, and the electrode wire is used for dragging the electrode plate, so that the electrode plate and the withdrawing catheter are matched with each other and are curled and contracted in the withdrawing catheter. Surgical operations such as laminectomy or laminotomy are not needed in the implanting operation process, the invasive property is small, trauma and operation risks are reduced, and the sheet-shaped electrode plates are not prone to displacement. In addition, the electrode plate can be withdrawn from the body along with the withdrawing catheter, and withdrawing and recycling of the electrode plate are achieved.

The utility model provides a split type kirschner wire and a kit for an orthopedic surgery robot, and belongs to the technical field of kirschner wires, the split type kirschner wire comprises a front kirschner wire body used for puncturing bones and a rear kirschner wire body used for being connected with an end effector of the orthopedic surgery robot, the front kirschner wire body is detachably connected with the rear kirschner wire body. Compared with Kirschner wire bending operation in the prior art, after the split type Kirschner wire is driven into the human body, the front Kirschner wire body with the proper length can be obtained more conveniently and safely, the problem of positioning displacement or loss caused by excessive pulling of the Kirschner wire is solved, and the Kirschner wire is more convenient to use. After the front kirschner wire body is detached and separated, due to the fact that the connecting end of the front kirschner wire body is smooth and clean, follow-up balloon dilatation kyphoplasty or pedicle screw implanting operation is facilitated, operation risks are reduced, and related operation operations can be carried out more safely, more reliably and more conveniently.

An insertion device for an ocular implant for regulating intraocular pressure includes a cannula having an internal space for receiving at least a portion of an ocular implant having a stent and an implant opening for inserting the ocular implant; a handle configured to be connected to the cannula and held by a surgeon; and a holder configured to be coupled to the handle and including a receiving portion configured to receive the stent of the ocular implant. The ocular implant insertion device appropriately fixes the stent inserted into the tube of the ocular implant in a manner attached to the insertion device, thereby preventing problems such as the stent coming out of the tube, the implant being separated from the insertion device by the stent, or the stent obscuring the surgeon's field of vision during implant implantation surgery.

The invention discloses a preparation method of a nano copper selenide antibacterial peptide-loaded multistage microporous titanium alloy. The preparation method comprises the following steps: 1, preparing a substrate; 2, surface modification; and 3, carrying out functionalization treatment to obtain the multistage microporous titanium alloy loaded with the nano copper selenide antibacterial peptide. The invention further provides the multistage microporous titanium alloy loaded with the nano copper selenide antibacterial peptide. The load design and photo-thermal synergistic mechanism of the nano copper selenide antibacterial peptide-loaded multistage microporous titanium alloy can effectively inhibit bacterial breeding and greatly reduce the infection risk of implantation operations, and on the aspect of promoting osseointegration, the multi-scale structure and ion slow release design can accelerate bone tissue growth and material fusion and reduce long-term complications, so that the titanium alloy can be used as a medical material for treating osteoporosis. The bone repair microenvironment is optimized, a new thought, good stability and safety are developed for complex disease treatment, long-term stable effect in vivo is guaranteed, strict standards are met, a solid foundation is laid for large-scale clinical application, and the bone implantation medical field is expected to be innovated.

The utility model provides a position adjusting instrument for an intraocular lens implantation operation of a lens eye, and relates to the field of ophthalmology medical instruments, the position adjusting instrument comprises a handle and a position adjusting hook acting piece; the position adjusting hook acting piece comprises a straight rod connected to the front end of the handle, a transition rod connected to the front end of the straight rod and a position adjusting rod connected to the front end of the transition rod. A first included angle alpha is formed between the transition rod and the straight rod; a position adjusting part is arranged at the front end of the position adjusting rod, and a second included angle beta is formed between the position adjusting rod and the transition part. According to the position adjusting instrument, through the unique structural design, the operation performance in a crystalline lens implantation operation is remarkably improved; wherein the position adjusting hook acting piece is composed of a straight rod, a transition rod and a position adjusting rod, and the operation position adjusting difficulty is effectively reduced through the specific angle design.

The application discloses a biological implant robot machining posture planning and error compensation method based on a global stiffness model, belongs to the technical field of biological manufacturing and surgical robot auxiliary machining, and comprises the following steps: a biomechanical stiffness atlas covering the whole posture space of the implant is constructed by sparse modal sampling combined with an inverse distance weighting algorithm. The application effectively solves the problem that the cell responses are inconsistent due to the machining quality differences of different regions of the complex curved surface implant through the global surface biological activity consistency, and significantly improves the long-term success rate of implant surgery. The application is easy to deploy on the existing medical robot through hardware pollution. Through micron-level functional molding, the micron-level biological texture depth is accurately controlled, and the manufacturing level of the personalized implant is improved from simple geometric shape customization to a new height of surface biological function customization.

The application provides a kind of composite multi-section structure medical catheter in technical field, including composite layer and bending wire, and bending wire is set through and out of composite layer.Composite layer includes inner tube layer and outer tube layer, and outer tube layer is set to wrap inner tube layer.Inner tube layer one end is connected to pull ring, and bending wire is set through and out of inner tube layer, and one end of bending wire is connected to pull ring, and the other end of bending wire is set out of one end of inner tube layer.Spring is set in outer tube layer, and spring is oppositely set outside inner tube layer.The application sets outer tube layer to wrap inner tube layer, and inner tube layer adopts three-section snake bone tube structure, which can reach different bending degree according to specific use requirement in different bending sections, such as head section, middle section and tail section, so as to guarantee the requirement of bending degree of each part of catheter in implantation operation, so that bending section can reach specific requirement bending degree.

The application discloses a kind of implant planning methods, comprising: collecting the relevant position parameters of implant implant position;Implant surgery robot with bone surface follow-up technology calculates the implant path according to the relevant position parameters;If there is no flap phenomenon, implant surgery robot executes the implant path completed by the completion of the planned completion, and completes implantation work;If there is a flap phenomenon, pause the implantation work of implant surgery robot, the problem that the flap situation encountered in the implant surgery process needs to be re-planned implant method is converted into the mathematical problem of coordinate transformation, and then the problem that implant surgery cannot be implemented according to the path planned in advance due to the phenomenon that flap is prone to appear in implant surgery process is solved by matrix transformation.

This utility model discloses a positionable dental implant healing abutment and a matching screwdriver. The positionable dental implant healing abutment includes an abutment body and a rubber column. An installation hole is formed at the center of the upper end face of the abutment body, and a connecting groove is formed below the installation hole, communicating with the installation hole. The rubber column includes a connecting section and a protruding section, with the connecting section installed within the connecting groove. The rubber column is connected to the abutment body via the connecting groove, preventing it from becoming loose. During the first-stage implant surgery, the rubber column can be trimmed according to the gingival height to make it flush with the gingiva, thus preventing impact on the integration of the implant and alveolar bone due to occlusal collision during implant healing. By setting the rubber column on the abutment body, it can be used to position the implant during the second-stage implant surgery, greatly reducing clinical operation time and avoiding incorrect incisions, as well as reducing the chance of bleeding and infection.

The utility model relates to the technical field of bone fetchers, in particular to a bone fetcher for tooth implantation, which comprises a connecting rod, a clamping groove and a stop guide component, the clamping groove is arranged on the inner side of the connecting rod, the stop guide component is fixedly connected with the tail end of the lower side of the connecting rod and comprises a stop plate, and a clamping hole is arranged on the inner side of the stop plate. The guide limiting assembly comprises a clamping pin, a limiting clamping ring is fixedly connected to the tail end of the lower side of the clamping pin, a rubber ring is arranged on the inner side of the limiting clamping ring, a fixing rod is fixedly connected to the outer side of the lower end of the limiting clamping ring, and a guide limiting ring is fixedly connected to the tail end of the lower side of the fixing rod. According to the bone meal collecting and storing device, the device can adapt to work at different angles, the phenomenon of deviation and inclination of the stopping ring is avoided, the bone meal collecting and storing effect and the rotating performance of a drill bit are guaranteed, and therefore the efficiency and safety of a dental implant operation are improved.

The disclosure provides compositions and methods for directing the growth of blood vessels in a tissue graft. The compositions and methods provide the advantage of directing the growth, size and pattern of blood vessels from the periphery of the graft, which recapitulates or improves the native blood vessel orientation in the host tissue. The compositions comprise a tissue graft that comprises a matrix attached to a barrier. The barrier comprises a porous membrane that permits passage of water and nutrients but blocks blood vessel growth. The methods comprise implanting the tissue graft on a host tissue in a subject and incubating the graft on the host tissue such that blood vessels grow around the edges (periphery) of the barrier or through intentional internal openings in the barrier and into the matrix. The methods can further comprise transplanting the vascularized tissue graft to a second location in the subject. Thus, the methods can be used in a staged implant procedure to create autologous, vascularized bioengineered tissue grafts.

An exemplary system comprises a memory that stores instructions and a processor communicatively coupled to the memory and configured to execute the instructions to perform a process. The process may comprise accessing an individual three-dimensional (“3D”) cochlea model of a cochlea of a recipient of a cochlear implant system that includes a stimulating lead inserted into the cochlea during a lead insertion procedure, generating, based on the individual 3D cochlea model and procedure data associated with one or more lead insertion procedures performed with respect to one or more other recipients, an individualized drug delivery profile for the recipient, and transmitting a command to the cochlear implant system to cause release of a drug from the stimulating lead in accordance with the individualized drug delivery profile.

The instant disclosure is directed to implantable electrospun structures for the delivery of active agents. An electrospun structure may comprise a first sheet and a second sheet. The first sheet and the second sheet may each comprise two supporting layers and an inner layer positioned between the two supporting layers, wherein a perimeter of one supporting layer is affixed to a perimeter of the other supporting layer, encasing the inner layer. The supporting layers may comprise a co-electrospun polymer fiber composition, and each inner layer may comprise an active agent blend-electrospun with a polymer fiber composition. All but one edge of the first sheet may be affixed to all but one edge of the second sheet, forming the electrospun structure, which may be a pouch. A method of using the pouch may comprise implanting it in a surgical site and, optionally, placing a medical device in the pouch.

The utility model discloses a tooth loss implantation model, and relates to the technical field of dental models, the tooth loss implantation model comprises a simulation jaw body, a plurality of simulation teeth are fixedly arranged at the positions corresponding to the teeth, and a loss groove is formed in the tooth loss position; the simulated gingiva is adhered to the simulated jaw body and is arranged at the missing groove in an avoiding manner; the simulated prosthesis is stuffed into the missing groove, a gingival layer is adhered to the top of the simulated prosthesis, and the gingival layer and the simulated gingival are made of the same material. The method has the effect of reducing the practice cost of the implant surgery for tooth loss.

The utility model belongs to the technical field of medical instruments, and particularly relates to a dental drill for implant surgery, which comprises a drill handle and a drill body arranged at one end of the drill handle, the drill body is provided with a plurality of blades axially and spirally distributed, and the blades converge on the end face far away from the drill handle to form an invasion cutting portion with taper. The cutting edges form a chambering part extending spirally on the cambered surface of the drill body, and end chip grooves with the number smaller than that of the cutting edges are formed in the cutting part. The axial end of the drill body is provided with the cutting blade with taper, the inclined groove for cuttings to invade is formed in the hole opening of the pre-formed small hole, so that the dental drill can smoothly drill into the pre-formed small hole, the blade is prevented from being clamped in the small hole, the cutting part is provided with the end chip grooves with the number unequal to that of the blade, and the blade back with the axial compression area unequal to that of the blade is arranged, so that the tooth drill can smoothly drill into the pre-formed small hole. The blades on the invasion cutting part are subjected to different axial pressures, and single blade concentrated stress is formed by using the pressure difference, so that the invasion efficiency is improved.

A non‑invasive, externally worn sling‑type device is disclosed for mitigating female urinary and fecal incontinence. The device comprises a hip‑encircling belt and a vertical support strap assembly configured to apply controlled external pressure to the external urethral meatus and the anal orifice. The vertical support strap assembly includes an anterior strap portion, a central support member seamlessly integrated between the anterior and posterior strap portions, and a posterior strap portion adjustably coupled to the hip‑encircling belt via a single G‑hook anchor and flat attachment loop at the central rear of the hip‑encircling belt. This configuration permits an initial, one‑time customized adjustment of the length and tension of the vertical support strap assembly. All components are preferably formed of the same medical‑grade thermoplastic elastomer (TPE) selected for hypoallergenic properties and durability. The device provides discreet mitigation of incontinence without internal insertion, surgical intervention, or absorbent pads, and is adaptable to varied anatomies and body types.

Novel tools and techniques are provided for implementing intelligent assistance (“IA”) or extended intelligence (“EI”) ecosystem to placement procedures for cardiac implantable electronic device (“CIED”). In various embodiments, a computing system might analyze received one or more first layer input data (i.e., room content-based data) and received one or more second layer input data (i.e., patient and / or tool-based data), and might generate one or more recommendations for guiding a medical professional in performing a CIED placement procedure in a heart of the patient, based at least in part on the analysis, the generated one or more recommendations comprising 3D or 4D mapped guides toward, in, and around the heart of the patient. The computing system might then generate one or more XR images, based at least in part on the generated one or more recommendations, and might present the generated one or more XR images using a UX device.

This invention discloses a method for optimizing and simulating dental implant design based on AI simulation technology, belonging to the field of artificial intelligence simulation technology in oral medicine. The method includes acquiring three-dimensional scans of the patient's oral cavity and jawbone images, fusing and reconstructing them to generate a personalized digital oral model. The model is then input into a pre-trained biomechanical simulation AI agent. This AI agent automatically explores within a solution space composed of multiple preset candidate implant models and combinations of implantation pose parameters. For each candidate scheme, dynamic mechanical load simulation is performed in the digital model, simulating stress distribution, bone interface micro-strain, and long-term stability indicators under different chewing conditions. Based on the simulation results, a multi-objective evaluation is performed to generate a comprehensive score. The scheme with the highest score is selected as the initial optimization design, and a surgical planning blueprint is generated. This invention achieves automated and intelligent optimization of implant surgery plans and quantitative prediction of biomechanical prognosis.

The present disclosure relates to valve replacement devices that are foldable for catheter-based deployment to the site of implantation, as well as systems for the delivery of valve prostheses, including prostheses having the special characteristics of the disclosed valve replacement devices. The devices include highly effective adhering mechanisms for secure and enduring precision implantation. The adhering mechanisms may employ a unique sealing mechanism that includes a cuff that expands slowly whereby the device is not secured in place until the completion of the implantation procedure. The implanted device, optionally together with the cuff, prevents perivalvular leaks and incorporate an appropriate leaflet system for reliable functioning in situ.

The invention discloses a guide plate device for auxiliary implantation of a 3D printing personalized planting carrier, and relates to the field of medical instruments for false tooth planting, an implantation sleeve is fixed in the middle of a guide plate, a positioning structure for insertion and positioning of a carrier body is arranged in the implantation sleeve, a screw is in threaded connection with the interior of the carrier body, and the screw is in threaded connection with the guide plate. A rod body of the screw coincides with the central axis of the carrying body, and a personalized implant is arranged below the carrying body; the guide plate is printed in a 3D mode, the guide plate is made of medical photosensitive resin and can be matched with teeth of a patient, the guide plate is fixed in the oral cavity, and in the sexual dental implant operation in-place process, the guide plate can guide an implant to be implanted according to the correct direction angle, so that the implant is implanted into an ideal site. The step-shaped platform at the bottom end of the personalized implant can shoot CBCT (cone beam computed tomography) before an operation and design height to limit the implantation depth of the implant, and the depth can be accurately controlled.

The utility model belongs to the technical field of medical instruments, and discloses a depth limiter. The depth limiter comprises a main body and a locking piece, the main body comprises a first abutting part and a second abutting part, and a clamping space used for containing an electrode wire is formed between the first abutting part and the second abutting part; the locking piece is connected with the main body, and the locking piece can extrude the first abutting part and / or the second abutting part, so that the first abutting part and the second abutting part tightly press the electrode wire in the clamping space. According to the utility model, the problem that the electrode lead is large in stress and easy to deform due to small stress area of the locking screw when the electrode lead is pressed down by the locking screw for locking can be solved; the problem that as the pressure of the locking screw on the electrode is gradually increased, the locking screw abuts against the surface of the electrode wire and rotates on the surface of the electrode wire to damage the surface of the electrode wire can be solved; the electrical stimulation stability between the electrode and the brain tissue is ensured, and the treatment effect is improved; and the implantation operation feeling of a patient is improved.

The utility model discloses a kind of injector of injection with suture artificial lens, specifically related to medical instrument field.The utility model provides a kind of injector of injection with suture artificial lens, including injector body, push rod, crystal cabin, injection pipe, automatic injection device, injector body is equipped with injection pipeline, push rod is set in injection pipeline, crystal cabin is detachably set in the front end of injector body, inner cavity for placing artificial lens is equipped in crystal cabin, the top of inner cavity is equipped with first suture slot for accommodating artificial lens suture, injection pipe is set in the front end of crystal cabin, second suture slot for accommodating artificial lens suture is equipped in injection pipe, second suture slot is connected with first suture slot, automatic injection device is set in the tail end of injector body, automatic injection device is connected with push rod for driving push rod to move in injection pipeline to implant artificial lens in surgical site.

1. Name of this design product: Occlusal positioning screw for implant restoration of edentulous jaws. 2. Purpose of this design: To assist in positioning the occlusal height during implant surgery. 3. The key design feature of this product is its shape. 4. The image or photograph that best illustrates the design's key points: a 3D model.

A system and method for use during an implant procedure during which a delivery system is being used to implant a leadless pacemaker (LP) within a patient may, while the delivery system is being used to position the LP at a potential implant site within the patient: receive, from the LP, data comprising one or more pacing impedance measurements and at least one measurement obtained by the LP other than pacing impedance; provide the data to a model that is produced prior to the implant procedure based on data collected from other patients; and use the model to output an indication of whether the LP should be chronically implanted at the potential implant site.

Systems and methods are disclosed for conducting spinal cord stimulation or other neurostimulation and sensing evoked compound action potential (ECAP) signals. The sensed signals may be processed to isolate ECAP features from noise and / or interfering signals. The isolated ECAP features may be used to control neurostimulation therapy for the patient, such as to quantify or measure lead migration and adjust a neurostimulation therapy for the patient to account for an impact of any detected lead migration, or other purposes (e.g., to guide an implant procedure).

This invention discloses an implanter capable of simultaneously implanting a bone anchor, a patch, and sutures, comprising: a drive rod, one end of which is adapted to and inserted into the head end of the bone anchor; the drive rod wall has a stepped winding shaft section for winding the patch; a sleeve, which is fitted onto the drive rod, one end of which can abut against the head end face of the bone anchor; the patch and the bone anchor are connected by a first suture, and the patch also has a second suture for connecting with tendon soft tissue. This implanter can simultaneously implant the patch, bone anchor, and sutures into the human body, then fix the bone anchor to the hard bone tissue, and finally fix the patch to the soft tissue through the second suture, eliminating the patch fixation step. This allows the implantation of the bone anchor, patch, and sutures to be completed in one procedure with the drive rod, simplifying the surgical procedure and saving the surgeon's surgical time.

A system for heart valve replacement surgery includes a guidewire and an elongated member. The elongated member has a side port located proximally at a distal apex of the elongated member. The guidewire is slidably disposed within a first lumen of the elongated member and configured to extend from the side port near the leaflet of the patient's natural heart valve. The side port includes an angled wall at its distal end, the angled wall being configured such that when the guidewire extends from the side port, it extends outward at an angle relative to the elongated member.

The utility model belongs to the technical field of medical instruments, and discloses an auxiliary tool. The auxiliary tool comprises a clamping part, the clamping part is provided with an installation channel extending in the first direction, the installation channel is used for containing a wire, and the clamping part applies one or more of friction force, resistance in the axial direction of the wire and pressure in the radial direction of the wire to the wire through the inner wall of the installation channel so that the clamping part can clamp the wire. According to the utility model, the original soft wire can keep certain rigidity under the action of the clamping part, the axial force application conduction of the wire is enhanced in the axial direction of the wire, when a user inserts the wire into a butt joint channel, the wire cannot be bent, twisted and locally deformed due to stress, and the efficiency, the safety and the reliability of an implantation operation are improved.