Abstract: The present disclosure provides a description of systems and methods for creation of a product formulary for medical product items. A clinical usage hierarchy is created for a practice area that includes multiple organizational levels and substitutable group categories. Data for known, categorizable products is entered into the categories of the clinical usage hierarchy and used to train a machine learning model, which is then deployed on a universal item database to populate the clinical usage hierarchy with all possible substitute items according to available categorization information in the database. This resulting clinical usage hierarchy has populated categories of items used in procedures in the practice area, where each item in a category is substitutable for any other item in that category, and is used to generate a product formulary utilized by physician or healthcare providers when selecting items for a future medical procedure in the practice area.

Abstract: The present disclosure relates to single tooth or full arch dental restoration. In cases where patients have insufficient bone stock for conventional root-form dental implants, current solutions often fail to restore function. The present disclosure describes a transalveolar dental implant for single tooth or full arch dental restoration. The transalveolar dental implant is comprised of a post and a bone plate, the bone plate having a contoured portion fabricated to match the topography of a bony surface of the facial skeleton. Through primary fixation of the contoured portion of the bone plate, the transalveolar dental implant improves function and outcomes in affected patients.

Abstract: Methods for manufacturing anatomical healing caps, including forming an anatomical healing cuff body for a given tooth position, the anatomical healing cuff body having a cross-section and an exterior surface so that the anatomical healing cuff body provides substantially custom filling of at least an emergence portion of a void where a natural tooth once emerged from the void or where a tooth would have emerged from a void of the given tooth position, and forming both lateral buccal and lingual handle extensions extending from the anatomical healing cuff body so that the manufactured anatomical healing cap includes a laterally extending buccal handle extension and an oppositely disposed laterally extending lingual handle extension, the buccal and lingual handle extensions being integrally formed with the healing cuff body. The healing caps can be formed using a casting jig, by machining, by 3D printing, or other suitable methods.

Abstract: Methods for manufacturing anatomical healing caps, including forming an anatomical healing cuff body for a given tooth position, the anatomical healing cuff body having a cross-section and an exterior surface so that the anatomical healing cuff body provides substantially custom filling of at least an emergence portion of a void where a natural tooth once emerged from the void or where a tooth would have emerged from a void of the given tooth position, and forming both lateral buccal and lingual handle extensions extending from the anatomical healing cuff body so that the manufactured anatomical healing cap includes a laterally extending buccal handle extension and an oppositely disposed laterally extending lingual handle extension, the buccal and lingual handle extensions being integrally formed with the healing cuff body. The healing caps can be formed using a casting jig, by machining, by 3D printing, or other suitable methods.

Abstract: Methods and dental prosthetics for providing soft tissue adhesion to a temporary healing abutment, or other dental prosthetic (e.g., temporary or permanent). Existing prosthetics generally do not provide any significant adhesion of the soft tissue surrounding the prosthetic, to the outer surface of the prosthetic itself. Because of the presence of gaps between such structures, or simple non-adhesion even where the structures may touch (but be free and unattached relative to one another), there is a tendency for pathogenic microbes to enter into such space between the structures, and for the soft gingival tissue to recede, particularly in patients with “thin” type periodontal tissue. The present disclosure provides materials and/or surface treatment (e.g., texturing) that ensures good bonding between the prosthetic and the soft tissue, reducing risk of infection, and reducing undesirable gingival recession surrounding the prosthetic anchored on a dental implant.

Abstract: Anatomical healing abutments, kits and methods for promoting healing of gingival tissue around a subgingival void of a given tooth position. The abutment includes a cuff body having an anatomical subgingival portion extending from an implant end to the gingival margin of the patient, and an emergent crown portion extending occlusally from the subgingival portion beyond the gingival margin. A directional alignment body may be disposed on the cuff body and configured to extend bucally beyond an outer perimeter of the cuff body when the cuff body is anatomically aligned relative to the void. The subgingival portion has an asymmetric cross-section and is occlusally flared to anatomically fill the void and support gingival tissue around the void to minimize slump of tissue into the void. The crown portion has a mesial-distal width that spans a width of the gingival margin and an occlusal height to extend beyond the gingival margin.

Abstract: Casting jigs, methods, and kits that may be used in manufacture of anatomical healing caps. A casting jig may include a body having one or more wells within the body, each well being open at a proximal end thereof and having a negative shape corresponding to an anatomical healing cuff body of a given tooth position. The casting jig includes an opening through the bottom surface through which an elongate handle may be inserted, allowing a temporary abutment to be coupled into the distal end of the elongate handle, so that the abutment is disposed in the well, held in place by the handle, as it is used as a core about which the anatomical healing cuff body is formed. A crown forming jig for forming an inexpensive, chair-side prepared bis-acrylic temporary crown that may be easily and quickly installed over the anatomical healing cuff body is also disclosed.

Abstract: Dental implants including radiopaque markers provided therein or thereon. The implant may also include customizable length characteristics. For example, a kit may include implants with different diameters (e.g., 3 diameters), where all of the implants are of a single (e.g., long) length. The appropriate diameter implant may be selected from the kit by the practitioner, and the long length implant may be cut (e.g., with a dental drill) to the appropriate length needed. The implants include radiopaque markers on or within the implant. For example, three series of markers may be provided on different “faces” of the implant, so that the three series of markers serve as reference points when scanning, allowing triangulation of the exact position of the implant in relation to the surrounding hard and soft oral tissues.

Abstract: A method of taking a scan of a patient's oral cavity may include providing an anatomical healing cap that can be received within a subgingival void of a given tooth position. The method may also include taking a first scan (e.g., an extraoral scan) of the anatomical healing cap before seating the anatomical healing cap into the subgingival void of the given tooth position, where the anatomical healing cap is coupled to an implant disposed adjacent the anatomical healing cap. Further, the method can involve taking a second scan (e.g., an intraoral scan) of the anatomical healing cap and surrounding surfaces, and then integrating the two scans into an overall oral cavity scan. Reference points from the first scan may be used to align the second scan with the first scan, integrating the two together.

Abstract: A first implant may be configured for attachment to a talus bone. A second implant may be configured for attachment to a calcaneus bone. The first implant attached to the talus bone can move in relation to the second implant attached to the calcaneus bone. A sheet can be disposed between the first implant and the second implant to facilitate relative motion between the first implant and the second implant. The sheet may provide a curvilinear surface that engages a curvilinear surface of the first implant or a curvilinear surface of the second implant to facilitate the relative motion. A set of tools may be used to distract the talus bone from the calcaneus, which may be used for insertion of the implants.

Abstract: A flexible abutment is provided to allow a prosthetic tooth or other dental device to simulate the flexibility of a natural tooth to provide protection from accidental sudden forces affecting the implant and allows for connection between a natural tooth and the implant, such as by a bridge.

Abstract: A failsafe driver mechanism is provided that protects a dental implant from damage.