Provided herein is an implant made of a biocompatible ceramic of synthetic origin obtained by additive manufacturing. The implant may include a dense portion featuring a material density by volume greater than 70%, and a porous portion connected to the dense portion by a connection zone. The porous portion may have an average macroporosity having a material density ranging from 30% to 70% by volume and cavities defining cavity sections, with a diameter ranging from 0.3 mm to 1.2 mm. The dense portion and the porous portion may define an external surface. The cavities may open onto the external surface.

A device and method for accelerating the conversion of oral bone graft to alveolar bone following extraction in a patient includes a vibrational dental device having a mouthpiece for contacting the dentition. Instructions are provided for using the vibrational dental device by placing the mouthpiece over the dentition, applying a vibratory force during a predetermined number of sessions throughout a predetermined treatment period, wherein the conversion of bone graft material to mature bone is enhanced and/or accelerated compared to without vibratory treatment.

A method for configuring a surgical guide and an associated implant. The implant and surgical guide are for maxillofacial osteosynthesis. Three-dimensional models of the pre- and post-operative anatomy are used to define attachment points. These attachment points are used to determine a structure for the implant and surgical guide.

The present invention relates to a dental implant for supporting, in particular by using a support structure, a cover element. The dental implant comprises a connection element having first and second end sections for connecting the dental implant to an implantation site of a jawbone and a first support element for supporting a cover element of at least a section of the implantation site after implanting the dental implant. The first end section is designed as, or comprises, a first connection section. The first support element comprises a second connection section. The first and second connection sections may be interconnectable. The second end section is designed as, or comprises, an implantation section for the temporary implantation of the connection element on or in the implantation site.

A system (1) for modifying a human or animal bone (2) is intended to reliably enable bone augmentation or bone reduction of the bone (2) to be treated in a particularly simple and, in particular, also particularly well-tolerated manner. For this purpose, according to the invention, a two-dimensionally extended lifting/pressure element (4) for insertion between the periosteum (6) of the bone (2) to be treated and the underlying bone (2) or the overlying connective tissue and a control element (10) associated therewith are provided, the control element (10) being designed to exert a magnetic pressure or tensile force on the lifting/pressure element (4).

A method for producing a bone replacement, a cavity or a bone being detected in a fully automated manner and the bone replacement being produced based on the detection also in a fully automated manner. It is also possible to produce information in relation to medical instruments or navigation information in a fully automated manner.

A bone implant including a wire mesh support frame having a plurality of interconnected wire members and at least two fastening points in the form of retention eyelets connected to the support frame by at least one of the wire members, and a biocompatible plate formed about the support frame, the plate having a bore associated with each of the retention eyelets.

A maxillofacial orthognathic fixation implant assembly and its method of production and use, the implant being an assembly of an upper anchor implant member, a lower anchor implant member and at least one bridging implant member, the anchor implant members being adapted to be securely mounted to a maxilla and the at least one bridging implant member being adapted to connect the upper anchor implant member to the lower anchor implant member in a fixed and rigid manner. With the anchor implant members affixed to the maxilla and the maxilla surgically separated between the upper and lower anchor implant members to create a lower portion detached an upper portion, the at least one bridging implant member is connected between the upper and lower anchor implant members to secure and maintain the lower portion of the maxilla in a desired post-operative position relative to the upper portion of the maxilla.

The present embodiment relates generally to methods of performing surgical technique maxillary sinus floor augmentation with a lateral approach using a pre-portioned and ready pre-packaged bone graft composition in gelatin bags and method of producing gelatin bags. In addition the present inventions can be widely used in other medical fields such as dentistry, orthopedic surgery, spine surgery, plastic and reconstruction surgery, sport medicine, trauma surgery, phinoplasty surgery and veterinary.

Various embodiments of implant systems and related apparatus, and methods of operating the same are described herein. In various embodiments, an intermedullary implant for interfacing with a bone structure includes a web structure, including a space truss, configured to interface with human bone tissue. The space truss includes two or more planar truss units having a plurality of struts joined at nodes. Implants are optimized for the expected stress applied at the bone structure site.