A method of preparing a device. The method includes fitting the device onto a first jaw of a patient, the device having a platform contoured for contact with teeth of the first jaw, identifying a set of contact areas between the device and teeth of a second jaw of the patient when the first and second jaws are moved towards each other, shaping, adjusting and/or trimming the device on the basis of the set of contact areas to change a location of at least one contact area, and repeating the preceding steps to bring the contact areas to or towards a desired configuration.

An ear splint for an ear is provided having a central portion having an exterior surface defining a first topology that is configured to dwell within an anterior scaphoid section of an ear, and a wing portion extending from the central portion and integrally formed therewith and at least partially surrounding an outer periphery of the central portion. The wing portion includes an exterior surface defining a second topology and is configured to be positioned along a postauricular area of the ear. The first magnetic device is disposed in the central portion and the second magnetic device is disposed in the wing portion. The magnetic retention feature exert a magnetic attractive force between the central portion and the wing portion such that at least a portion of the exterior surface of the central portion and at least a portion of the exterior surface of the wing portion contact the ear.

An anatomical brace for dynamically stabilizing the elbow during elbow articulation, the anatomical brace comprising: a brace body comprising a distal portion for fitting over the forearm of a user and a proximal portion for fitting over the upper arm of a user; a hinge mechanism comprising a distal segment, a proximal segment and a pivot for pivotally connecting the distal segment and the proximal segment, the distal segment of the hinge mechanism being mounted to the distal portion of the brace body and the proximal segment of the hinge mechanism being mounted to the proximal portion of the brace body; a pivot cable guide mounted to the anterior portion of the pivot; an upper arm cable guide mounted to at least one of the proximal segment of the hinge mechanism and the proximal portion of the brace body, the upper arm cable guide being configured to change the direction of a cable extending through the upper arm cable guide; an ulnar collateral ligament (UCL) cable guide mounted to the brace body and configured to direct a cable extending through the ulnar collateral ligament (UCL) cable guide over the ulnar collateral ligament (UCL) and toward the distal portion of the brace body; and a cable having a first end and a second end; the first end of the cable being mounted to the distal segment of the hinge mechanism, the second end of the cable being mounted to the distal portion of the brace body, and the cable being routed proximally along the distal segment of the hinge mechanism, through the pivot cable guide, proximally along the proximal segment of the hinge mechanism, through the upper arm cable guide, and through the ulnar collateral ligament (UCL) cable guide; wherein, when the anatomical brace is mounted to the arm of a user so that the distal portion of the brace body is secured to the forearm of the user, and the proximal portion of the brace body is secured to the upper arm of the user, and when the elbow thereafter moves to full extension, the cable is tensioned, whereby to apply a force to the ulnar collateral ligament (UCL) of the user, and when the elbow thereafter moves to full flexion, the cable is relaxed, so that the force applied to the ulnar collateral ligament (UCL) is released.

A foldable pelvic binding device and method of use is provided. The device includes a main body divided into a plurality of panels and segments by a grid of living hinges, thereby facilitating movement between stowed and flat configurations. The main body is configured to couple with one or more other main body, as necessary or desired, to create a binding device that is sized for the required application, thereby accommodating a variety of applications in a variety of situations for a variety of body shapes and sizes. By engaging the binding device with a tourniquet, a binding system is created. When not in use, each the main body of the binding device can be moved to the stowable configuration by folding the various panels over each other.

A foldable pelvic binding device and method of use is provided. The device includes a main body divided into a plurality of panels and segments by a grid of living hinges, thereby facilitating movement between stowed and flat configurations. The main body is configured to couple with one or more other main body, as necessary or desired, to create a binding device that is sized for the required application, thereby accommodating a variety of applications in a variety of situations for a variety of body shapes and sizes. By engaging the binding device with a tourniquet, a binding system is created. When not in use, each the main body of the binding device can be moved to the stowable configuration by folding the various panels over each other.

Systems and methods are disclosed that relate to a stabilization and cooling apparatus having a stabilizing structure with at least one inflatable chamber, the stabilizing structure configured to become semi-rigid upon inflation of the at least one inflatable chamber. A cooling structure is integrated with the stabilizing structure and includes a single-use cooling element and a thermally conductive material in thermal communication with the single-use cooling element. The apparatus also has an actuator configured to cause inflation of at least one inflatable chamber.

A flat foot orthosis has two bodies and a pelvis portion. Each one of the two bodies has a wearing space, a foot portion, an ankle portion, a shank portion, a knee portion, a thigh portion, a toe portion, a hallux valgus region, a substrate, a first elastomer, and a second elastomer. The substrate and the first elastomer are disposed adjacent to each other, and surround the wearing space. The substrate extends from the toe portion to the thigh portion. The first elastomer spirally extends from an instep of the foot portion to the thigh portion through the rest. The two first elastomers surround and fetter where the wearer's pelvis and the wearer's waist meet. The second elastomer extends from the hallux sheath, is connected to the first elastomer, and wraps over the hallux valgus region.

A medical apparatus including a bar with a first attachment loop, a second attachment and a plurality of hooks, wherein the medical apparatus is an arch bar.

A conformable body interface is fabricated using a data set representing a three-dimensional, soft tissue body surface. The conformable body interface includes a body scaffold that is divided into two or more longitudinal segments separated by axial joints. Optionally, the body scaffold is further divided into two or more circumferentially split segments separated by circumferential joints. The axial joints are circumferentially constrained by elastic bands, tabs, or similar structures and the circumferential joints are longitudinally constrained by elastic axial tethers or similar structures. In this way, the body interfaces can accommodate swelling and bending of the body surface.

Systems, methods, and devices are described for providing a fluid control for an inflation system. The control directs fluid flow from an inlet to one or more outlets of the control. The outlets are independently connected in fluid communication with the inlet by through the control. The control allows a user to create a fluid path between the inlet and a selected outlet by positioning the control in an orientation corresponding to the desired outlet. Each outlet is independently connected in fluid communication with the inlet in various orientations of the control.