934results about "3D printing" patented technology

An expandable intervertebral implant may include a superior endplate configured to engage a superior vertebra, and an inferior endplate configured to engage an inferior vertebra, wherein the inferior endplate may be spaced apart from the superior endplate by a gap. The expandable intervertebral implant may further include a first slider moveable along a first direction to urge linear expansion of the gap, and one or more cams each coupled to the first slider. The one or more cams may be configured to urge angular expansion of the gap in response to at least one of: rotation of the one or more cams about a rotation axis, and motion of the one or more cams along the first direction.

An expandable intervertebral implant may include a superior endplate configured to engage a superior vertebra, and an inferior endplate configured to engage an inferior vertebra, wherein the inferior endplate may be spaced apart from the superior endplate by a gap. The expandable intervertebral implant may further include a first slider moveable along a first direction to urge linear expansion of the gap, and one or more cams each coupled to the first slider. The one or more cams may be configured to urge angular expansion of the gap in response to at least one of: rotation of the one or more cams about a rotation axis, and motion of the one or more cams along the first direction.

The embodiments provide various interbody fusion spacers, or cages, for insertion between adjacent vertebrae. The cages may have integrated ratchet assemblies that allow the cage to change size and angle as needed, with little effort. The cages may have a first, insertion configuration characterized by a reduced size to facilitate insertion through a narrow access passage and into the intervertebral space. The cages may be inserted in a first, reduced size and then expanded to a second, larger size once implanted. In their second configuration, the cages are able to maintain the proper disc height and stabilize the spine by restoring sagittal balance and alignment. Additionally, the intervertebral cages are configured to be able to adjust the angle of lordosis, and can accommodate larger lordotic angles in their second, expanded configuration. Further, these cages may promote fusion to further enhance spine stability by immobilizing the adjacent vertebral bodies.

A sacroiliac fusion implant device assembly has an implant body and a pair of bone fasteners. The implant body has a distal end and a proximal end with a longitudinal axis extending between a center of the distal end and a center of the proximal end. The distal end has cutting edges configured to cut tissue as the implant is pressed into a joint between a sacrum and an ilium. The proximal end has two bone fastener receiving apertures, each configured to receive a bone fastener and the implant body has a pair of sidewalls connecting the distal and proximal ends. The pair of bone fasteners can be a pair of threaded fasteners, or a pair of spike fasteners or a combination of one threaded fastener and one spike fastener.

Computer implemented methods, systems, and computer products employing program code or algorithms for use in customized patient specific hip implants or femoral stems or sleeves having an outer surface that corresponds more closely to the inner surface of the cortical bone of a patient's femur compared to conventional hip implant or femoral stems or sleeves based on population-based design.

A bellows shaped spinal implant, comprising an upper plate, a lower plate and a bellows shaped shell extending between and joining the upper and lower plates. The bellows shaped shell is formed of titanium or an alloy comprising titanium and includes a wall extending therearound that defines a hollow interior. The wall has a thickness in the range of 0.5 mm to 1.0 mm to provide for radiographic imaging through the wall. The wall is angled or curved inwardly or outwardly between the upper and lower plates to provide stiffness mimicking the stiffness properties of a similarly sized polyetheretherketone (PEEK) implant. The upper and lower plates each comprise porous contact regions including a three-dimensional gyroid lattice structure defined by a plurality of struts and pores in communication with the hollow interior. The outer surfaces of at least a portion of the struts may comprise a laser ablated textured surface.

A system and computer-implemented method for manufacturing an orthopedic implant involves analyzing tissue characteristics based on image data of anatomy. Image data of a patient can be analyzed to identify at least one tissue characteristic at different locations along anatomic elements of anatomy of interest. A patient-specific implant configuration can be determined based on the analysis of the image data of a patient.

Systems and methods for designing and implementing patient-specific surgical procedures and / or medical devices are disclosed. In some embodiments, a method includes receiving a patient data set of a patient. The patient data set is compared to a plurality of reference patient data sets, wherein each of the plurality of reference patient data sets is associated with a corresponding reference patient. A subset of the plurality of reference patient data sets is selected based, at least partly, on similarity to the patient data set and treatment outcome of the corresponding reference patient. Based on the selected subset, at least one surgical procedure or medical device design for treating the patient is generated.

The invention relates to a bionic meniscus 3D printing method and system, and the method comprises the steps: reading a meniscus STL model, carrying out the data preprocessing of the data of the model, and carrying out the construction to obtain a concave envelope contour; performing offset processing and four-curve segmentation to generate an elliptic equation fiber field; establishing a bidirectional mapping relation between a parameter space of an elliptic equation fiber field and a meniscus physical space based on an RBF mapping theory; based on a meniscus fiber density gradient change theory, performing simulation in a parameter space of the elliptic equation fiber field to obtain a bionic gradient fiber field; according to the meniscus STL model, the bidirectional mapping relation and the bionic gradient fiber field, fiber path coordinates of a meniscus physical space are obtained, and a 3D printing path is generated; and printing according to the 3D printing path to obtain the bionic meniscus. Precise simulation of a natural meniscus complex fiber structure is achieved through mathematical modeling, and the technical problems that in the prior art, fiber field control precision is insufficient, and regional characteristics are difficult to achieve are solved.

The invention relates to a computer-implemented method for adjusting a position of artificial teeth of a denture. A digital 3D model of the denture comprising at least a denture part is provided. The denture part is configured for a jaw of a patient and comprises a dental arch with a plurality of artificial teeth arranged in an artificial gingiva. A deformable gingiva section of the artificial gingiva is defined between the teeth of the plurality of artificial teeth and a fixed gingiva section of the artificial gingiva with a fixed geometrical form. The dental arch is moved as a whole relative to the fixed gingiva section in order to adjust the position of the dental arch. A geometrical form of the deformable gingiva section is deformed due to the moving of the dental arch, whereas the fixed gingiva section maintains the fixed geometrical form.

The present disclosure relates to computer-implemented methods (100) for generating a virtual model of a first section of bone tissue including cortical bone tissue. The method comprises (104) obtaining microstructural cortical parameters including an indication of a number of osteons (210) and of a cross-sectional area of the osteons, a number of lamellae (212) forming the osteons, an indication of locations of osteons in the section of bone tissue and of dominance of the osteons. The method further comprises generating a virtual model using a generative design algorithm comprising (1061) defining a geometric space, (1062) generating a cortical cloud of points, (1064) segmenting the geometric space into substantially circular regions, defining an outer surface of the osteons. The method further comprises (1065) forming consecutive substantially concentric surfaces corresponding to the lamellae until the obtained virtual model satisfies boundary conditions formed by the microstructural cortical parameters.

The invention discloses an improved wedging cage within the sacroiliac (SI) joint and fixation screw(s). The wedging cage is adapted to be positioned between the sacrum and the lilac bone (e.g., the sacroiliac joint), and the wedging cage is effective to receive one or more fixation or axial screws to fasten the wedging cage and secure the wedging cage to the adjacent pelvic bones to provide a combination effect of fusion and / or fixation. Accordingly, the improved fixation screw assemblies promote flexibility and adaptability due to the adjustable head being movable to a locked and unlocked position relative to the screw body when implanted onto a substrate.

Methods, systems, and techniques for collecting data for use in designing a personalized dental prosthesis for a patient. At least one camera is used to obtain a series of two-dimensional photos or a three-dimensional model of a head and face of the patient. At least one machine learning model is used to determine facial or oral landmarks and a central incisal edge of the prosthesis from the photos or model. Dimensions for the dental prosthesis are determined form the landmarks and central incisal edge. The dimensions include a labial border of the prosthesis, distal borders of the prosthesis, a superior border of the prosthesis, an inferior border of the prosthesis, a lingual border of the prosthesis, and buccal borders of the prosthesis. The dimensions are output to an output file for use in manufacturing the prosthesis.

The invention provides an interbody fusion cage and a manufacturing method of the interbody fusion cage. The interbody fusion cage comprises a first end plate assembly, a second end plate assembly and an elastic supporting assembly. The two ends of the elastic supporting assembly are connected with the first end plate assembly and the second end plate assembly respectively. The first end plate assembly comprises an end plate body, a tooth retreating prevention structure and a porous structure, the end face of one end of the end plate body is connected with the elastic supporting assembly, and the end face of the other end of the end plate body is a bearing contact face used for abutting against vertebra tissue; the tooth retreating prevention structure and the porous structure are respectively arranged on the bearing contact surface; the tooth retreating prevention structure protrudes out of the bearing contact surface and is used for being fixedly connected with vertebra tissue; hollowed-out holes are formed in the porous structure and used for allowing a part of growing vertebra tissue to extend into the porous structure. The interbody fusion cage solves the problems that in the prior art, due to the fact that the contact area between an interbody fusion cage and vertebrae is small, postoperative prostheses are prone to disengagement or looseness, end plate sclerotin is damaged, and the fusion efficiency is poor.

A sacroiliac (SI) joint implant assembly addresses SI joint dysfunction and degenerative sacroiliitis. The assembly includes a first implant body, a second implant body, and a piezoelectric layer positioned between them. The piezoelectric layer generates electrical charges when subjected to mechanical stress, stimulating bone growth and enhancing stability of the SI joint after surgery. The implant bodies may feature non-planar surfaces to distribute compressive and shear forces unevenly across the piezoelectric layer. The assembly can be secured using fasteners such as screws, pins, or brackets, and may include porous or fenestrated bodies made from materials like titanium or polymers. Some implant assemblies are designed for minimally invasive surgical procedures, with configurations that allow for precise placement using guide wires and imaging techniques. The assembly aims to stabilize the SI joint and promote bone fusion, leveraging the piezoelectric effect to improve the overall efficacy of the fusion procedure.

The invention discloses a dental restoration customization system combining 3D printing with digital modeling, and particularly relates to the technical field of digital modeling, the dental restoration customization system comprises an oral cavity scanning module, a data fusion module, an occlusion mechanical analysis module, a restoration optimization module, a 3D printing module and a feedback monitoring module, the digital model is generated and transmitted to the data fusion module, the data fusion module integrates oral cavity scanning, medical records and dental data to form a personalized oral cavity digital model, and the occlusion mechanical analysis module collects occlusion data, analyzes stress distribution and feeds back the stress distribution to the prosthesis optimization module. The dental restoration optimization module adjusts the design of the restoration according to the oral cavity structure and the occlusion relationship of the patient, the 3D printing module performs high-precision printing according to the optimization design to generate a personalized dental restoration, and the feedback monitoring module monitors the comfort of the restoration through a pressure sensor and feeds back a result to the restoration optimization module for real-time adjustment. And the optimal performance and comfort of the prosthesis are ensured.

The embodiment of the invention is suitable for the technical field of dentistry and 3D printing, and provides a method and system for manufacturing a dental object, the method comprises the following steps: obtaining a dental model, the dental model comprising at least one abutment and a repair part associated with a dental prosthesis model; establishing a stent model, wherein the stent model is configured to be mounted on an abutment tooth; a base model is established, the base model comprises a first part and a second part, the support model is clamped between the first part and the second part, and the first part of the base model is aligned with the repair part of the dental model; establishing a tooth prosthesis model, wherein the tooth prosthesis model is aligned with the second part of the denture model; manufacturing a base plate based on the first part and the second part of the base plate model, and manufacturing a stent based on the stent model; the base and the stent are connected to obtain a dental object. By adopting the method, the dental object can be manufactured in a digital mode, and the manufacturing efficiency and accuracy of the dental object are improved.

Provided herein are an anchor and interbody for interbody fusion, including an interbody for insertion between human vertebrae, including an interbody cage including a plurality of anchor receptacles, each anchor receptacle configured to receive an anchor to secure the interbody to a vertebra; and the anchor, including a head configured to engage an anchor receptacle; a curved partial-tubular shank with a convex curve, connected to or integral with the head at a distal end of the head, and extending from the head; a tapered tip portion extending from a distal end of the curved partial-tubular shank; one or more rails integral with or connected to an outside surface of the anchor, extending from a proximal end of head and along the curved partial-tubular shank to a proximal end of the tapered tip portion; and a feature formed from two flat surfaces on an outside of the anchor and a rail.

Compliant connectors can span gaps between support segments of an expandable implantable spinal device. The compliant connectors can lay flat when under strain in a stowed position and can expand to maintain an expanded configuration defined by the plurality of support segments when released. A minimally compact size and / or profile of the expandable implantable device may be achieved. which also achieving a relatively large size in the deployed configuration of the device.

The present disclosure relates to an artificial lumbar disc and provides a lateral approach artificial disc that is inserted laterally rather than anteriorly of the spine, thereby preventing damage to blood vessels or other organs that may occur when an anterior access artificial disc is inserted from the front, shortening the surgical time, preventing dislodgment of the artificial disc, and improving the surgical prognosis. The artificial disc is inserted between two adjacent vertebrae and includes an upper plate contacting an upper vertebra, a lower plate contacting a lower vertebra, and an inserter inserted between the upper plate and the lower plate to allow the upper plate to rotate by a set angle with respect to the lower plate, and an upper wing portion and a lower wing portion are formed on the upper plate and the lower plate.

In some embodiments, apparatuses and methods are provided herein useful to providing data files associated with orthodontic appliances. In some embodiments, a system for providing data files associated with orthodontic appliances comprises a database, wherein the database stores the data files associated with the orthodontic appliances and a control circuit, wherein the control circuit is communicatively coupled to the database, a user device, and a printer, wherein the control circuit is configured to receive, from the user device, an indication of a selected orthodontic device, retrieve, based on the indication of the selected orthodontic device from the database, one of the data files associated with the orthodontic appliances, wherein the one of the data files associated with the orthodontic appliances corresponds to the selected orthodontic appliance, and transmit, to the printer, the one of the data files associated with the orthodontic appliances.

The invention relates to a 3D printing porous metal-ceramic assembled composite implant as well as a preparation method and application thereof. The 3D printing porous metal-ceramic assembled composite implant comprises a porous metal-ceramic implant body formed by compounding a 3D printing integrated porous metal module and a 3D printing integrated porous ceramic module, the porous metal-ceramic implant body and the net-shaped metal protection body are arranged on the periphery of the porous metal-ceramic implant body in a wrapping mode, and the assembled composite implant can be accurately matched with the appearance and the combination surface of bone tissue of a defect part. The composite implant disclosed by the invention has osteogenesis environment regulation and control functionalization, and can achieve the effects of immediately recovering the movement function of defective bone tissue, improving the tissue microenvironment of a bone defect part, accelerating new bone regeneration and guiding new bone to grow towards the interior of the porous metal implant, so that rapid osseointegration of a bone / metal implant interface is realized; and the long-term treatment effect of 3D printing porous metal implant / autologous bone fusion type repair after ceramic degradation is achieved.

A spinal implant device includes a unitary strand extending from a first end to a second end. The unitary strand includes an exterior surface defining an infill volume with an infill structure. The exterior surface extends from the first end to the second end. A first bead is formed in the strand has a first diameter. The second bead is formed in the strand has a second diameter. At least one joint is formed in the strand between the first bead and the second bead. The at least one joint has a third diameter that is less than the first diameter and less than the second diameter.

A patellar prosthesis includes a support component in metallic material and a joint cap in polymeric material, anchored to an anchoring surface of said support component.

The invention discloses a design method of a structural mechanical gradient regulation and control interbody fusion cage for end plate defects. The design method comprises the following steps of data acquisition and model construction; analyzing the shape of the defective end plate; carrying out interface mechanical adaptation design on the defect end plate and the structural gradient fusion cage; performing multi-objective optimization; the invention relates to a 3D printing defect endplate mechanical and biological adaptive spinal fusion cage. The individual end plate defect model can be established according to the difference of different patients, the local elastic modulus of the fusion cage is dynamically adjusted through morphological analysis and typing, the stress conduction height matching with the defect end plate is realized, the settlement risk is reduced, and the fusion effect is improved; by combining the biological adaptation design of the end plate, the pore structure and material characteristics of the fusion cage are optimized, and bone healing is promoted; through the scheme of image analysis, digital design, intelligent optimization and precise manufacturing, a mechanical and biological dual-adaptive fusion cage system solution is provided for a patient with the defect of the end plate.

The present invention relates to methods for curing polymeric dental appliances comprised of partially cured photopolymerizable components, especially for additively manufactured denture base and artificial tooth components utilized in the production of full and partial dental prostheses. In particular, the invention relates to methods of utilizing a curing apparatus having one or more controllable heating sources and one or more controllable LED light sources to achieve specific preheating and light curing conditions for more effectively converting partially cured photopolymerizable components from a partially cured state to a final cured state.

An orthopaedic joint replacement system is shown and described. The system includes a number of prosthetic components configured to be implanted into a patient's knee. The system also includes a number of surgical instruments configured for use in preparing the bones of the patient's knee to receive the implants. A number of methods for using the surgical instruments to prepare the bones is also disclosed.

The present invention relates to a method for using a lyophilization hyaline cartilage powder to produce a composition for regenerating cartilage, and a composition for regenerating cartilage produced by using the method, the method comprising: A) a step for preparing hyaline cartilage; B) a step for freeze-drying and crushing the hyaline cartilage, and producing a lyophilization hyaline cartilage powder; C) a step for producing an adipose tissue extract from autologous adipose tissue; and D) a step for producing a composition which is for regenerating cartilage and including the lyophilization hyaline cartilage powder and the adipose tissue extract.

The present invention relates to a medical device manufactured using the additive manufacturing process (3D printing). It is a medical device used preferably as a bone graft composed of a porous structure based on bioceramics based on β-tricalcium phosphate (β-TCP) or hydroxyapatite, which may or not contain nanostructures in its composition, for example: carbon nanostructures (graphene, graphene oxide, reduced graphene oxide, carbon nanotubes, etc.) and, in preferred embodiments, stem cells and polymeric membrane. Also, the present invention relates to the use of this device as a bone graft and the process of preparing this device.

Implant systems and methods treatment of a joint include a distal portion, a middle portion, and a proximal portion. The distal portion may include a thread having a first thread minor, a first thread major, and a first pitch. The distal portion also may have a reverse cut, helical fenestration formed through the thread. The middle portion may be devoid of threads and may include a porous outer surface structure to promote bony integration, the porous outer surface structure having a leading end and a trailing end, with the leading end having a diameter larger than the first thread minor. The proximal portion may include a proximal thread having a second thread minor, a second thread major, and a second pitch. The second thread minor may be substantially the same width as the trailing end of the middle portion.