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.

A method of implementing a splint device, and associated splint device, are provided for a guidance system of a surgical robot. A splint body includes first and second stabilizing portions extending from opposed lateral sides of a medial portion, and defines a U channel. The medial portion, or the medial portion and one of the stabilizing portions, defines a bridge portion extending along the U channel. A partition member, received by the bridge portion, extends into and longitudinally along the U channel. An adhesive material is engaged with the splint body, within the U channel. The U channel is engaged about a tooth or jaw of a patient, and urged toward the tooth or jaw, such that the partition member engages the tooth or jaw and separates the adhesive material into a first portion engaged with the first stabilizing portion and a second portion engaged with the second stabilizing portion.

The present invention relates to a tooth-borne guide plate, a mucosa-borne guide plate, a bone-borne guide plate, and preparation and application methods therefor. The method for preparing a tooth-borne guide plate comprises: a) bonding a radiopaque material to teeth, bonding the radiopaque material to the gingival mucosa or/and bonding the radiopaque material to other anatomical features; b) performing CBCT photography, and acquiring CBCT data with radiopaque material information; c) acquiring oral cavity surface STL data with radiopaque material information; d) matching the CBCT data with the STL data; e) determining the positions of an implant and a retention pin; f) generating a base guide plate; g) generating an in-place guide plate; h) generating an implant guide plate; and i) generating a repair guide plate. By means of the tooth-borne guide plate, the mucosa-borne guide plate, the bone-borne guide plate, and the preparation and application methods therefor provided in the present invention, the precision and success rate of data matching can be improved, thereby improving the patient's comfort, reducing the number of subsequent visits, and reducing clinical medical costs.

A dental implement is disclosed that includes a proximal end portion; a distal end portion that includes a cutting head defining at least one cutting surface; and a guide body that is positioned proximally of the cutting head. The guide body defines at least one flute that extends in generally parallel relation to a longitudinal axis of the dental implement and is configured to direct irrigation fluid to a surgical site within a patient.

Ablation probe tips (108, 148, 320, 360) and physical and virtual stents (110) for use in tooth bud ablation procedures that result in tooth agenesis as well as tooth bud ablation methods are described herein.

An ablation procedure. The ablation procedure may be applied to tooth buds 120 and result in tooth agenesis. The ablation procedure may be applied to lesions or tumors. A tooth bud ablation system for use in a tooth bud ablation procedure that results in tooth agenesis. A method for volume scanning both hard tissues and soft tissues of a patient. A method for manufacturing or fabricating a custom surgical stent 110. A custom surgical stent 110 for use in a tooth bud ablation procedure that results in tooth agenesis, the custom surgical stent 110 for use with an ablation probe tip 108 having a center of ablation 130a.

A first guide member includes a horizontal body portion and a pair of upright portions. The horizontal body portion has an arcuate configuration and includes a first horizontal surface, a front surface, a rear surface, and a second horizontal surface. The first horizontal surface is flat. The first upright body portion includes a first inwardly extending portion. A first engagement surface of the first inwardly extending portion is configured to rest on a ridge of the alveolar arch of the patient. The second upright body portion includes a second inwardly extending portion. A second engagement surface of the second inwardly extending portion is configured to rest on a ridge of the alveolar arch of the patient. The first guide member lacks a component configured to extend along a lingual or palatal side of the alveolar arch of the patient.

A splint device (100) for robotically-guided surgery includes elongate first and second splint portions (200, 400) each having opposed longitudinal ends and an interface edge extending between the ends, wherein the respective interface edges (250, 450) are arranged as a complement to each other. First and second alignment elements (800A, 800B) engaged with the first and second splint portions are arranged to interact with each other such that a substantially consistent gap is defined between the first and second interface edges, from the first ends to the second ends of the first and second splint portions. A threaded member (900) is engaged between the first and second splint portions and arranged to advance the first and second interface edges toward each other in response to advancement of the threaded member. A tracking portion (1000) having a kinematic mount (1100) engaged therewith is engaged with the first or second splint portion and extends outwardly therefrom. An associated method is also provided.

A tracking and guidance arrangement for a surgical robot system and related method are provided. The arrangement includes a patient-interacting device including an instrument engaged a distal end of a guide arm and a fiducial marker coupled to maxillofacial anatomy of the patient. A detector is connected to an articulating arm and co-operable therewith to be positioned adjacent to the fiducial marker, with the detector being configured to interact with the fiducial marker. A controller device is configured to receive data from the detector relative to the interaction thereof with the fiducial marker, to determine a spatial relation between the fiducial marker and the detector based on the data, to determine a spatial relation of the instrument relative to the fiducial marker, and to direct the instrument to interact with the maxillofacial anatomy of the patient according to the determined spatial relations.

A dental implant includes an insertion portion which extends along an implant axis, and a coronal projection for receiving an abutment having a dental prosthesis formed thereon, which can be mounted on the dental implant with a screw. The insertion portion includes a coronal region and an apical region. The coronal projection extends from the coronal region of the insertion portion in the coronal direction and along a prosthesis axis. The coronal projection and the insertion portion are integrally connected in one piece. The prosthesis axis and the implant axis are inclined towards each other, and the abutment having the dental prosthesis formed thereon is attachable to the dental implant with only one screwing operation in the direction of the prosthesis axis.