A prosthetic device includes a first material and a second material that surrounds a least a portion of the perimeter of the first material. The first material and the second material have a resting shape that is configured to fit a body part on which the prosthetic devices is to be implanted. The second material is deformable to fit the prosthetic device through an opening of the subject smaller than the resting shape to reach the body part. A prosthetic device can be produced by obtaining image data corresponding to a body part of the subject, generating and refining one or more models of a body part based on the image data, and producing the prosthetic device as a three-dimensional print of the refined model.

An artificial bone plate unit and an assemblable artificial bone plate are provided. The artificial bone plate unit includes a plate body, multiple connecting pins and multiple connecting holes. The plate body has two main surfaces and a peripheral surface. The peripheral surface is connected between the two main surfaces. The connecting pins and the connecting holes are formed on the plate body and along the peripheral surface on the plate body. The connecting holes correspond in shape to the connecting pins. The assemblable artificial bone plate is bendable and includes multiple artificial bone plate units. The artificial bone plate units are connected using the connecting pins and the connecting holes. The assemblable artificial bone plate is assembled from artificial bone plate units and then bent into the shape of the defect area of the skull, which saves material and time.

An implant and guide are described, together with methods for configuring the same. The implant and guide are for maxillofacial osteosynthesis and may be provided as a kit. Three-dimensional models of the pre- and post-operative anatomy are used to define attachment points. These attachment points are used to define a structure for the implant and the guide.

A method and apparatus for whole-mind cognitive interface. Such a system includes a bodily-integrated artificial cranium, computer, RF antenna, and transceiver array to seamlessly augment the human brain with artificial intelligence (AI) and permit enhanced cognitive functions, and human host feed-back-based neurological rewiring.

A medical device comprising a substantially flexible porous structure. The porous structure comprises a plurality of interlocking units. Each of the plurality of interlocking units comprises a body and at least one arm. The plurality of interlocking units is configured to have space between adjacent interlocking units when the porous structure is in a neutral configuration. The plurality of interlocking units is configured to contact the respective body and arm of adjacent interlocking units when a compressive force is applied to the porous structure, thereby restricting compression of the porous structure. The plurality of interlocking units is configured to contact the respective arms of adjacent interlocking units when an extension force is applied to the porous structure, thereby restricting extension of the porous structure.

Resorbable implants, coverings and receptacles comprising poly(butylene succinate) and copolymers thereof have been developed. The implants are preferably sterilized, and contain less than 20 endotoxin units per device as determined by the limulus amebocyte lysate (LAL) assay, and are particularly suitable for use in procedures where prolonged strength retention is necessary, and can include one or more bioactive agents. The implants may be made from fibers and meshes of poly(butylene succinate) and copolymers thereof, or by 3d printing molding, pultrusion or other melt or solvent processing method. The implants, or the fibers preset therein, may be oriented. These coverings and receptacles may be used to hold, or partially/fully cover, devices such as pacemakers and neurostimulators. The coverings, receptacles and implants described herein, may be made from meshes, webs, lattices, non-wovens, films, fibers, foams, molded, pultruded, machined and 3D printed forms.

Resorbable implants, coverings and receptacles comprising poly(butylene succinate) and copolymers thereof have been developed. The implants are preferably sterilized, and contain less than 20 endotoxin units per device as determined by the limulus amebocyte lysate (LAL) assay, and are particularly suitable for use in procedures where prolonged strength retention is necessary, and can include one or more bioactive agents. The implants may be made from fibers and meshes of poly(butylene succinate) and copolymers thereof, or by 3d printing molding, pultrusion or other melt or solvent processing method. The implants, or the fibers preset therein, may be oriented. These coverings and receptacles may be used to hold, or partially/fully cover, devices such as pacemakers and neurostimulators. The coverings, receptacles and implants described herein, may be made from meshes, webs, lattices, non-wovens, films, fibers, foams, molded, pultruded, machined and 3D printed forms.

The present invention is directed to methods for collecting and processing autografts, processed autografts, kits for collecting and transporting autografts, and tools for preparing autografts. It is also directed to autologous bone grafts, and methods of preparing them.

Methods, devices and systems for virtual, remote and real-time collaboration between surgeons and engineers using system learning and intelligent and timely disbursement of design and performance information to engineering teams embarking on the preliminary design event of a personalized orthopaedic implant or personalize surgical instrument utilizing a case-based reasoning expert system. Additive manufacturing technology and statistically controlled advanced manufacturing processes quickly produce personalized medical devices worldwide.

A method for corrective surgery with a rearrangement of skeletal features, such as facial skeletal features, of a patient and a refinement of irregularities by alloplastic implant in a single surgery. The method includes determining whether the patient is a candidate for corrective surgery and pre-operatively imaging skeletal features to be rearranged to produce three-dimensional computer renderings of the skeletal features. The rearrangement of skeletal features is pre-operatively planned, and skeletal irregularities to remain after the rearrangement of skeletal features are pre-operatively predicted. Based on the skeletal irregularity predicted to remain after the rearrangement of skeletal features, an alloplastic implant is pre-operatively designed and manufactured by computer-aided design and manufacture. In a single surgery, skeletal features are rearranged in accordance with the pre-operative planning, and the alloplastic implant is applied to the skeletal features in correction of the predicted skeletal irregularity.