A mobile bearing prosthetic implant may include a fossa implant seated in the fossa cavity of the skull and secured to the zygomatic arch. The fossa implant may define a primary recess constructed and arranged to mimic the articular eminence of the temporal bone such that a floating bearing connected to a ramus implant may translate along the original path that the condylar head would take during movement of the jaw. The floating bearing may be constructed and arranged to move from the first jaw angle recess to the second jaw angle recess and is positionable therebetween such that a longitudinal axis of the floating bearing is perpendicular to the direction of movement of the floating bearing within the fossa implant.

The application is directed to devices and methods where one or more magnetic or magnetizable implants provides therapeutic benefits to a patient. The implant may be useful for expanding the range of motion of joints or dynamically providing different responses to changing conditions in the body where the implant is placed. An electromagnet is placed on or in a bone on one side of a joint, and another electromagnet or magnetically active material is placed on or in a bone on the opposing side of the joint. The electromagnet may be continuously energized to relieve pressure in the joint space, or may be energized in response to forces applied to the joint.

A temporomandibular joint replacement system includes a condylar component secured with a mandibular bone and a fossa component with a fossa backing secured with a zygomatic bone, the fossa having an open-ended concave fossa dome with a post-center peak to allow for mediolateral and anterior translation with a rounded, oblong condylar head of the condylar component. The bone-interfacing surfaces are anatomically-contoured to their respective bone surfaces and formed with materials and textures which promote osseointegration with the joint replacement.

A temporomandibular joint replacement system includes a condylar component secured with a mandibular bone and a fossa component with a fossa backing secured with a zygomatic bone and slidably attached with a removable fossa lining, the fossa lining having an open-ended concave fossa dome with a post-center peak to allow for mediolateral and anterior translation with a rounded, oblong condylar head of the condylar component. The slidable attachment mechanism of the fossa backing and fossa lining is laterally-oriented to allow for post-implantation removal and replacement without disturbing any bone or bone-interfacing components. The bone-interfacing surfaces are anatomically-contoured to their respective bone surfaces and formed with materials and textures which promote osseointegration with the joint replacement.

An Apparatus for an Anatomical Prosthesis of the Temporomandibular Joint which includes a polymeric centralizing device for the pyriform condyle in the concavity of the polymeric temporal section that joins the condyle to the body of the mandibular fixture, in a stable and secure way, using a frictional interference Cone-Morse-Connection, as well as a flat part in the center of the cavity of the temporal section and posterior edges of specific dimensions, which make the fixture of the junction of the mandibular section and the temporal section more secure and allows freedom of centric movement.

A prosthesis for at least a portion of a bone, in particular a bone or portion thereof to which, in the natural condition, a tendon of a muscle is attached, wherein the prosthesis is manufactured of a metal or an alloy thereof and is provided with at least one area situated in the surface of the prosthesis that faces outward once the prosthesis has been placed in the body, the area being formed by a layer provided with open spaces that are connected to each other, wherein the open spaces are dimensioned for allowing the growth of bone tissue therein.

A patient-specific artificial temporomandibular joint is proposed. The patient-specific artificial temporomandibular joint includes: a temporal bone coupling part including a fixing body that is fixed to the temporal bone of a patient and a head receiver that is detachably coupled to the fixing body and provides a close-contact curved surface being open downward; and a mandible coupling part including a coupling body that is fixed to the mandible of a patient and a head that has a spherical shape and is supported by the coupling body in contact with the close-contact curved surface of the head receiver. The patient-specific artificial temporomandibular joint is manufactured by 3-D printing on the basis of shape data of the temporal bone or the mandible of a patient, so a good implanting effect is provided and the patient quickly recovers. Further, worn parts can be partially replaced, thus there is a little burden of maintenance.

An anatomically-shaped, human bone graft may be cultivated ex vivo using a bioreactor capable of perfusing large complex porous scaffolds. Scaffolds derived from image-based modeling of a target are seeded with human mesenchymal stem cells and cultivated. A bioreactor configured to house complex three-dimensional scaffold geometries provides controlled flow for perfusion of the cells. Dense uniform cellular growth can be attained throughout the entire scaffold as a result of the medium perfusion. In an embodiment, the bioreactor has a mold into which perfusion medium is pumped under pressure and multiple ports through which the medium exits the mold.

Prosthetic device (10) for temporomandibular joint comprising a first prosthetic component (11), able to be associated with a mandibular condyle (112) of a patient, and a coordinated second prosthetic component (12), able to be associated with a respective glenoid fossa of the patient.

The present invention also concerns a guide device (35) for making an anchoring seating (113) for positioning the first component, and a prosthetic assembly comprising the prosthetic device (10) and the guide device (35).

The application is directed to devices and methods where one or more magnetic or magnetizable implants provides therapeutic benefits to a patient. The implant may be useful for expanding the range of motion of joints or dynamically providing different responses to changing conditions in the body where the implant is placed. An electromagnet is placed on or in a bone on one side of a joint, and another electromagnet or magnetically active material is placed on or in a bone on the opposing side of the joint. The electromagnet may be continuously energized to relieve pressure in the joint space, or may, be energized in response to forces applied to the joint.