Patent classifications
A61F2/30942
Patient-specific mandibular implant inserted into mandibular defect region and method of manufacturing the same
Disclosed is a patient-specific mandibular implant inserted into a mandibular defect region and a method of manufacturing the same, and more particularly, to a patient-specific mandibular implant inserted into a mandibular defect region, which can be easily and rapidly manufactured using personalized three-dimensional (3D) printing technology for a defect region, can provide an effect of preparing a later step for restoring a tooth in advance, and can be easily manufactured tooth restoration data based on the Korean standard database (DB), and a method of manufacturing the same.
3D MODELING SYSTEMS AND METHODS
Systems and methods for creating a geometric design definition for 3D models designed to fit physical or digital template objects is disclosed. The 3D models can transform to fit specific physical or digital objects which are different from but topologically isomorphic to the original template objects based on visual or mathematical inputs. To validate the fit, the generated 3D model can be compared with the specific physical or digital objects for which the 3D model is generated to fit, and the geometry of generated 3D model can be adjusted to improve the fit if the generated 3D model is not validated. The accuracy of the fit of the generated 3D models can be improved iteratively.
Method for 3-D printing a custom bone graft
A method for producing bone grafts using 3-D printing is employed using a 3-D image of a graft location to produce a 3-D model of the graft. This is printed using a 3-D printer and a printing medium that produces a porous, biocompatible, biodegradable material that is conducive to osteoinduction. For example, the printing medium may be PCL, PLLA, PGLA, or another approved biocompatible polymer. In addition such a method may be useful for cosmetic surgeries, reconstructive surgeries, and various techniques required by such procedures. Once the graft is placed, natural bone gradually replaces the graft.
Systems and methods for orthopedic implants
A system and computer-implemented method for manufacturing an orthopedic implant involves segmenting features in an image of anatomy. Anatomic elements can be isolated. Spatial relationships between the isolated anatomic elements can be manipulated. Negative space between anatomic elements is mapped before and/or after manipulating the spatial relationships. At least a portion of the negative space can be filled with a virtual implant. The virtual implant can be used to design and manufacture a physical implant.
CRANIOFACIAL IMPLANT INCLUDING A PASSIVE PRESSURE SENSOR
A craniofacial implant includes a craniofacial implant body and a passive pressure sensor. The craniofacial implant body permits measurement of the passive pressure sensor via externally applied stimuli passing through the craniofacial implant body.
SYSTEMS AND METHODS FOR PRE-OPERATIVE VISUALIZATION OF A JOINT
A method for displaying graphical indications associated with a joint includes: receiving image data associated with a joint of a subject; generating a three-dimensional model of at least a portion of the joint of the subject using the image data; identifying at least one region of the joint that deviates from a baseline anatomy by comparing at least a portion of the three-dimensional model to a baseline model; generating at least one measurement of a characteristic of the joint at one or more predefined locations using the three-dimensional model and a coordinate system; displaying a spectrum bar graph that comprises at least one representation of the at least one measurement of the characteristic of the joint; determining a pathology associated with the joint based on the at least one measurement of the characteristic of the joint; and displaying at least one graphical indication indicating the pathology associated with the joint.
Method for producing a tailor-made implant
A method for producing a tailor-made implant intended to be implanted at an implantation site of a damaged bone part, the method comprising a step in which a 3D representation of a standard implant is superposed on a 3D representation of a damaged bone part by positioning said standard implant on an implantation site of the damaged bone part, in order, if necessary, to modify the dimensions and/or to adjust the shape of said standard implant, and also, if necessary, to modify the outer surface of said standard implant, which may be either the impression or substantially the impression of the outer surface of said bone part in the state prior to superpositioning of said implant, when the geometry of the damaged bone part is intended to be retained, or a functional outer surface, when said tailor-made implant is intended to be used at the interface of two bone parts cooperating with each other.
System and method for fabricating cartilage implants
A system and method used to fabricate an implant from cartilage, where the implant can be used in reconstructive surgery. The system includes a thermoregulation device capable of maintaining a desired temperature range during milling operations. The milling machine is controlled by instructions generated from a digital model of the implant. The digital model can be a stock model or a custom model created from medical scans.
SYSTEMS, METHODS AND DEVICES FOR REPLACEMENT OF THE TEMPOROMANDIBULAR 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.
REPLACEABLE FOSSA COMPONENT FOR A TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM
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.