A reference member for determining a position of an implant analog can comprise a trapezoidal body including a first side and a substantially parallel second side. The first side can define a first dimension and the second side can define a second dimension that is greater than the first dimension.

A treatment element for use with a dental-implant part anchored in a patient's jawbone is disclosed, wherein the treatment element includes a base body having a connection system adapted to the dental-implant part for mechanical connection of the base body with the dental-implant part, and at least one media duct for conducting a cleaning liquid.

Methods and apparatus for transmitting vibrations via an electronic and/or transducer assembly through a tooth or teeth are disclosed herein. The assembly may be attached, adhered, or otherwise embedded into or upon a removable oral appliance to form a hearing aid assembly. Such an oral appliance may be a custom-made device. The electronic and transducer assembly may receive incoming sounds either directly or through a receiver to process and amplify the signals and transmit the processed sounds via a vibrating transducer element coupled to a tooth or other bone structure, such as the maxillary, mandibular, or palatine bone structure.

The present invention relates to a system and method for dental implant and restorative services. By locating the key functions at one physical location, dental implant services are efficiently provided to patients. These functions include a treatment coordinator, a direct marketer, a restorative doctor/prosthodontist, a surgeon, an imaging area, and a dental laboratory, Further, services for dentate patients are improved by utilizing advanced dental implant methods and systems. These methods and systems include both model-based services and CT (computed tomography) guided surgery services. Using these services, improved surgical guides for dental implants are constructed.

A reference member for determining a position of an implant analog can comprise a trapezoidal body including a first side and a substantially parallel second side. The first side can define a first dimension and the second side can define a second dimension that is greater than the first dimension.

A horizontal transalveolar implant system designed to support dental implants in cases where vertical bone height is insufficient. The system features a linear anchor with a threaded body, a drilling tip, and a torque area. It includes transversal screw receiving apertures that hold removable sealing screws, which are replaced by threaded dental implant receivers after insertion. The system allows for secure attachment of abutments and dental crowns. This innovative design anchors lengthwise in the alveolus, eliminating the need for sinus lifts and possibly bone grafts, providing a stable foundation for dental restorations. The anchor measures approximately 30 to 35 mm in length and 3 to 4 mm in diameter, making it suitable for cases with minimal vertical bone availability.

In general, one aspect disclosed features a method comprising: providing a bone section; attaching a cutting guide to the bone section; cutting the bone section into multiple bone graft sections using the cutting guide; arranging the multiple bone graft sections in a neo-mandible position; attaching a temporary fixation plate to the multiple bone graft sections after arranging the multiple bone graft sections in the neo-mandible position; removing the cutting guide from the multiple bone graft sections after attaching the temporary fixation plate; attaching a final fixation plate to the multiple bone graft sections after removing the cutting guide; and removing the temporary fixation plate from the multiple bone graft sections after attaching the final fixation plate to create a neo-mandible assembly.

In various embodiments of the presently disclosed technology, a neo-mandible is provided. The neo-mandible may comprise: (1) a first bone graft; (2) a second bone graft abutting the first bone graft to form a triangular recess between the first and second bone grafts; and (3) a triangular plate attached to the first and second bone grafts, wherein the triangular plate is nested within the triangular recess between the first and second bone grafts such that the triangular plate does not protrude outside the triangular recess.

A method of installing a dental prosthesis that includes having a practitioner install at least one narrow implant and at least one standard implant into a subject's bone, where the narrow implant has a narrow implant abutment that is exposed after installation, and the standard implant has a standard implant abutment exposed after installation. The practitioner places a narrow implant housing over each narrow implant abutment, and places a standard implant housing over each standard implant abutment. The practitioner flows a resin within a channel located within a dental prosthesis and places the dental prosthesis over each narrow implant housing and each standard implant housing such that the resin surrounds each narrow implant housing and each standard implant housing. Once the resin cures, each narrow implant housing and each standard implant housing is fixed within the resin and the resin is fixed within the dental prosthesis.

A protocol for preparing and fitting a prosthetic in a prosthetic field of a patient using pre-surgical fiducial markers comprises obtaining pre-surgical physiologic data of the patient sufficient to create a base patient image of the prosthetic field; determining fiducial marker placement and placing fiducial markers in the determined fiducial marker placement in physiologic structure within the prosthetic field which is unchanged by planned surgery; optionally obtaining pre-surgical physiologic data of the patient with the fiducial markers in place sufficient to create a base patient image of the prosthetic field with fiducial markers; performing surgery; obtaining post-surgical physiologic data of the patient with the fiducial markers sufficient to create a post-surgical patient image of the prosthetic field with fiducial markers; manufacturing and fitting a final prosthetic based upon post-surgical patient image of the prosthetic field with fiducial markers. Registration images useful for the protocol are disclosed.