The invention relates to a method for operating an orthopedic device which supports or replaces a first body part of a wearer and has at least one controllable actuator, wherein the method includes a) determining a chronological profile of at least one parameter, which allows for a conclusion to be made regarding a movement status of the wearer, from measurement values of at least one sensor; b) detecting the movement status from the at least one determined chronological profile; and c) controlling the at least one controllable actuator depending on the identified movement status, wherein at least the chronological profile of at least one parameter of a second body part of the wearer is also used to identify the movement status.

An improvement to a prosthetic device which provides a spring member between first and second structural members that are rotatably connected to one another, the spring member providing predictable resistance as it is compressed by the rotation of the first and second structural members with respect to each other. The known resistance of the spring is used as an input to a model controlling a motor control circuit to provide counter-torque as rotational torque is applied to compress the spring.

A gap-adjustable/eliminable shock absorption structure includes a shock-absorbing ankle body having a thread adjustment portion. An elastic body and a driving piston are provided on a spring carrier pivotally mounted inside the shock-absorbing ankle body. The driving piston is connected, through screwing, to an inverted T-shaped connector. A cylinder extending from the driving piston is fit into a friction bushing, such that a surface of the cylinder is closely fit to an inside surface of the friction bushing. The friction bushing has an oblique outside surface that is closely fit to an internal wall of the shock-absorbing ankle body. The thread adjustment portion receives a fastening ring and an adjusting ring to screw thereto such that fine adjustment is achieved through displacement caused by rotation of the adjusting ring to set up tight engagement with the friction bushing as being closely fit to the surface of cylinder surface.

An orthotic device for a patient's foot includes a shell that is configured to structurally support the patient's foot. The shell has a variable thickness along a dimension of the shell. The shell is configured to undergo flexion throughout the shell. The variable thickness of the shell targets areas of increased stress.

The joint device having a linking unit which links a first member and a second member in a manner allowing relative movement, and having an expansion/contraction device 12 which is connected across the first member 1 and the second member in a manner allowing power transmission and which can modify an angle formed by the first member and the second member around the linking member by expanding and contracting. The expansion/contraction device has a rotary unit which generates rotary power, and a conversion unit which is connected to the rotating unit in a manner allowing power transmission and converts the rotary power generated by the rotary unit into translational motion along a direction of expansion/contraction.

The invention relates to a method for controlling a prosthesis or orthesis of the lower extremity, which prosthesis or orthesis comprises an upper part (10) and a lower part (20) that is connected to the upper part (20) via a knee joint (1) and is mounted so as to be pivotable relative to the upper part (10) about a joint pin (15); wherein an adjustable resistance device (40) is situated between the upper part (10) and the lower part (20), by means of which resistance device a flexion resistance (Rf) in an early and middle standing phase is modified, during walking, on the basis of sensor data, following initial heel contact up to the middle standing phase; wherein, following the initial heel contact, the flexion resistance (Rf) is increased to a value at which further flexion is blocked or at least slowed; wherein the progression over time of the flexion resistance increase and/or the maximum achievable flexion angle (Af) is modified on the basis of the inclination of the ground or a height difference (ΔH) to be overcome.

Prosthetic coupling interfaces and methods of use are disclosed herein. An example system can include an external fixator apparatus, a prosthetic appendage assembly, and a prosthetic coupling interface for connecting the external fixator apparatus with the prosthetic appendage assembly.

A knee prosthesis system including a knee prosthesis, an actuator and a controlling unit. The knee prosthesis includes a thigh segment and a shank segment. The actuator rotatably connects the shank segment and the thigh segment. The actuator is configured to controllably assume a powered knee behavior to generate knee motion or a passive knee behavior to resist knee motion. The controlling unit includes a finite-state control structure. The controlling unit electrically communicates with the actuator. The control structure includes at least three passive states and at least one powered state. The passive states include a passive stance-resistance state, a swing-flexion state, and a swing-extension state and the at least one powered state includes at least one of a swing-assistance state, a stance-assistance state, and a powered-swing state.

Various examples are provided for modular prosthetic devices and their use. In one example, a device includes a chassis assembly including a joint portion; and an interchangeable module that can be removably attached to the chassis assembly. The interchangeable modules can be configured for use in a wide variety of applications. The interchangeable modules can be quickly exchanged for different activities.

A system for attachment of a device to a bone is provided. The system includes an internal axial rod with a proximal and distal end that is configured to be inserted and secured into a bone cavity’s distal end. The system can also include an internal-external transfer rod with a proximal and distal end mounted into the distal end of the axial rod and a central channel extending through the transfer rod from the proximal end to the distal end and a plurality of attachment rings for attaching at least one tissue or muscle group to the transfer rod. The system also includes a bio-compatible and bio-occlusive artificial membranes (BIOCAMS) lamina, wherein the lamina includes either a polyetheretherketone (PEEK) mesh, a biocompatible polymer, a carbon fiber polymer, an artificial tissue polymer, molded donor tissue, allogenic tissue, a collagen/hyaluronic acid-based tissue, or connective tissue biosynthetic substrate material suitable as webbing.