Abstract: A medical textile product includes a textile substrate having opposed first and second surfaces with the textile substrate including a textile construction of one or more yarns. The second surface includes a coating of a substantially water-insoluble, non-porous elastomeric sealant. The one or more yarns at the first surface are pre-treated with a removable composition, such that the water-insoluble elastomeric sealant encapsulates a portion of fibers of the one or more yarns at the second surface of the textile substrate. The textile substrate is substantially impermeable to fluid. The first surface is substantially free of the substantially water-insoluble elastomeric sealant. The textile substrate may be a non-tubular substrate, such as a planar sheet, a shaped sheet, and a tape, or a tubular substrate, such as a cylindrical conduit, a tubular conduit, a Y-shaped, a T-shaped conduit, a multi-channel conduit, and a bulbous shaped conduit.

Abstract: A bone insert includes a cap having a convex top surface made from a plurality of cap micro struts, an elongated stem made from a plurality of stem micro struts, and a barrier between the cap and the stem. The stem of the bone insert is inserted into a hole formed in a host bone until the barrier is pressed against the exposed bone. The bone implant can be placed against a small focus contact point on the cap. Liquid cement can be injected into a large center hole in the cap and the cement can flow through the fenestrations between all of the cap micro struts as well as the space between the bone implant and the bone. The cement can cure to create a high strength structure that provides a strong bond between the bone implant and the host bone.

Abstract: A system is disclosed herein for providing a kinetic assessment and preparation of a prosthetic joint comprising one or more prosthetic components. The system comprises a prosthetic component including sensors and circuitry configured to measure load, position of load on a curved surface, joint stability, range of motion, and impingement. In one embodiment, the system is for a ball and socket joint of a musculoskeletal system. The system further includes a computer having a display configured to graphical display quantitative measurement data to support rapid assimilation of the information. The kinetic assessment measures joint alignment under loading that will be similar to that of a final joint installation. The kinetic assessment can use trial or permanent prosthetic components. Furthermore, adjustments can be made to the applied load magnitude, position of load, and joint alignment by various means to fine-tune an installation.

Abstract: A delivery device for an annuloplasty implant is disclosed comprising an outer sheath, a delivery wire being movable within said sheath in a longitudinal direction thereof, a holder being releasably connectable to said implant, said holder being pivotably connected to a distal portion of said delivery wire, wherein said holder is folded inside said outer sheath in a delivery configuration, and wherein said holder is foldable from said delivery configuration to an expanded deployed configuration outside said outer sheath. A system comprising such delivery device and an annuloplasty implant, and a method of delivering such implant is also disclosed.

Abstract: The Nucleo-reticular Multi-cell Dual-system Eye Implant consists of a spherical structure with calculated and variable axial length depending on the needs required by the orbital eye socket, composed of a cell mesh with alternative designs that in turn, makes up the MMM System, in which suturing is provided in any technique, either in cases of evisceration or enucleation. Thanks to its multi-cell structural design, it favors its placement and reduces the risk of migration, extrusion, exposure and extraction. As it is an arrangement with structural holes, it provides a higher percentage of the volume for its vascularization; it also houses inside a Reticular Fibrovascular Core System, which has a structure based on multilevels equipped with micro-reticular tissue and an intra-level communication based on filaments; with the capacity to contain medicines and/or technology by presenting a dual-system of two screw-on pieces, being able to manufacture in different structural designs and biocompatible materials.

Abstract: The invention is directed to a system and methods for treating neurovascular compression. Certain preferred embodiments of the invention generally comprise an apparatus having an elongated body portion including a proximal anchor element and distal anchor element. The apparatus also may include one or more marker elements to facilitate placement of the apparatus by the user. The apparatus may be configured to permit the user, after insertion and deployment of the apparatus in a blood vessel, to move the blood vessel so that the blood vessel is no longer in contact with and compressing a nerve or other parts of the nervous system.

Abstract: A medical dressing is disclosed, the medical dressing has an adhesive layer having a skin-facing surface to adhere the medical dressing to a dermal surface, wherein said adhesive layer comprises a first chemical compound incorporated within said adhesive layer, and wherein at least a portion of said skin-facing surface has a coating comprising a second chemical compound. Also disclosed is a method of manufacturing such a medical dressing.

Abstract: A size adjustable cover used for soft tissue reinforcement which is adapted to envelop an implantable device, such as a breast implant, in a surgical application. The cover is formed using a circular two-dimensional implantable matrix material having an inner circle and a plurality of fringes which radiate circumferentially from the inner circle. The implantable device is positioned upon the inner circle, and the plurality of fringes are folded inwardly to form an overlapping implant pocket which envelops the implantable device. Each fringe further has a punched opening, allowing a loop of suture thread to link each fringe together. Certain fringes are excluded from the loop to create stabilization tabs which radiate from the inner circle and are attached to a site of host implantation to stabilize the cover and the implantable device within.

Abstract: The present invention relates to the diagnosis and treatment of joint-related diseases, in particular osteoarthritis. Based on the analysis of the microarchitecture, such as microchannels, of the subchondral bone, the present invention provides methods for evaluating the health state of a joint as well as determining whether a joint is prone to develop or has already developed a disease correlated to joint and cartilage destruction. The invention further provides for membranes and other implants mimicking healthy subchondral bone structure suitable for promoting regeneration of joint structure and function.

Abstract: An orthosis provides a wearer at least one of forearm supination, forearm pronation, shoulder internal rotation, shoulder external rotation, shoulder adduction, shoulder abduction, shoulder flexion, shoulder extension, elbow flexion, and elbow extension. It includes a shoulder assembly adapted to be secured to a wearer's shoulder and an upper arm assembly connected to the shoulder assembly and adapted to be secured around a wearer's upper arm. The upper arm assembly defines an upper arm assembly axis. A wrist assembly is adapted to be secured around a wearer's wrist. The wrist assembly defines a wrist assembly axis. A splint arm assembly includes an upper splint arm, a lower splint arm, and a pivot pivotally connecting the upper splint arm to the lower splint arm. The upper splint arm adjustably connects to the upper arm assembly and the lower split, arm adjustably connects to the wrist assembly.

Abstract: A cervical collar has a chin support slidably connected to an inside surface of an anterior component adapted to secure against an anterior chin and neck of a user. A posterior component connects to the anterior component to circumferentially surround the user's neck. A height adjustment mechanism has spring locks securing the height adjustment mechanism against the anterior component. The cervical collar includes a footplate continuously extending from the height adjustment mechanism generally without a variation in thickness. The posterior component has side portions with a plurality of living hinges located proximate to elongate slots for straps connecting to the anterior component.

Abstract: The Protective Cast Cover is a cover you wear over your cast. It is made of fabric, any kind of fabric, waterproof, warm, breathable, what ever kind of fabric will work for an individual's needs. For arms it covers the whole arm with a mitten hand over the top of the shoulder. Some of them are shirts, just depends on what the individual request. The cover for legs covers the foot to the top of thigh and can be made as pants, or as shorts on the opposite side of the leg with the cast. If they are in double casts, then both sides would be made the same. This works for arms or legs. Again, just depends on what the individual request. The protective cast cover is meant to keep sand, or debris or even water out of the cast, and give people less stress about their situation.

Abstract: The present invention relates to a male contraception apparatus for obtaining a time-limited sterility of a male mammalian individual. The apparatus comprises a restriction device adapted to restrict the lumen of a vas deferens of the mammalian, and a controller operable to control the restriction device to restrict the lumen of the vas deferens during a controlled period to prevent sperms from reaching the urethra of the mammalian. The apparatus further comprises an implantable constriction device configured to gently constrict at least one portion of a tissue wall of the vas deferens to restrict the lumen of the vas deferens such that the flow of sperms in the vas deferens is restricted, and a stimulation device configured to stimulate the constricted wall portion of the tissue wall.

Abstract: A grip strengthening device having a finger portion for enhancing the grip by means of at least one artificial tendon arranged along at least one finger portion, wherein the finger portion comprises material along both sides and a tip, and possible along a dorsal side, the at least one artificial tendon is attached along both sides so that the artificial tendon may move, wherein the artificial tendon runs closer to a ventral side than the dorsal side of the finger portion, at least at positions corresponding to joints of a wearer's finger, the finger portion will transfer a force to provide a movement of the finger when the artificial tendon is retracted, wherein the artificial tendon runs in a detour towards or to a position in the middle between the dorsal and ventral side or closer to the dorsal side at a proximal portion of the finger portion.

Abstract: A rear-entry ankle brace includes an elastomeric component defining an inside elbow channel configured to span an ankle joint. A channel opening extends the length of the elastomeric component for direct insertion on top of a leg. One or more leg straps are used to adjustably tension first and second rear edges of the channel opening toward one another and secure the brace to the lower leg. Two foot straps are used to adjustably tension first and second bottom edges of the channel opening toward one another and secure the brace to the mid-foot. The foot straps overlap on the bottom to define a plantar surface of the brace and cross over each other on the topside of the elastomeric component and are secured to a leg strap. A pair of stabilizing stirrups optionally are included on the inside surfaces of the elastomeric component and receive the malleoli.

Abstract: A compression garment includes a main body including a central portion and a plurality of straps that extend from the central portion. The central portion has a lateral edge having first regions from which the straps extend from the central portion, and second regions from which the straps do not extend. A connecting portion is fixed to the main body and is fixed to at least a portion of the second regions. The straps are moveable to reverse the compression garment between a first state and a second state. The straps may be moveable around the connecting portion, or may be feedable through the connecting portion, to reverse the compression garment between the first state and the second state. The connecting portion and the main body may define a plurality of slits through which the straps are insertable to reverse the compression garment.

Abstract: The diagnosed soft tissue or brain injury component of concussions is generally defined by the symptoms of the temporal lobe manifestations. However, there is an undiagnosed structural fractured component of concussions occurring within the jaw joint complex which is the focus of this invention. A precise imaging technique and the powerful 3D Cone beam scanning technology, together, have revealed fractures in temporal bones of the jaw joint space which supports the temporal lobe of the brain. These fractures are the results of the lower jaw impact forces that cause concussions and this mechanism account for a large percent of the concussions arising in sports and military operations. These fractures have never been considered, diagnosed, or treated in the management of concussions. Fracturing temporal bones in the jaw joint that supports the temporal lobe will certainly produce the symptoms of temporal lobe manifestations.

Abstract: Systems and methods for assessing compliance with position therapy. In an embodiment, position therapy is provided to a user while the user is wearing a position therapy device. The position therapy comprises, by the device, collecting positional data, determining positions of the user over a time period based on the positional data, and, when it is determined that the user is in a target position, providing feedback to the user to influence the user to change to a non-target position. In addition, the device stores a duration of use in its memory. The duration of use indicates a duration that the user has used the wearable position therapy device in each of one or more positions. An assessment of the user's compliance with the position therapy is then provided based, at least in part, on the duration of use.

Abstract: A distraction frame for use with a surgical table, wherein the surgical table includes a base for positioning on a floor, the distraction frame including a table mount for fixation to the base of the surgical table; at least one horizontal strut mounted to the table mount; at least one vertical strut mounted to the at least one horizontal strut; and at least one distraction mechanism mounted to the at least one vertical strut, wherein the at least one distraction mechanism may be connected to a limb of a patient for applying a distraction force to the limb of the patient; wherein the table mount may transfer to the floor a force moment imposed on the table mount when the at least one distraction mechanism applies a distraction force to a limb of a patient.

Abstract: A medical device may include an implantable device for treating a body tissue structure. The implantable device may include a plurality of bodies spaced from adjacent bodies and arranged so as to be configured to extend around an exterior surface of a body tissue structure. The bodies may be configured to apply a static force to the body tissue in a relaxed state and may adjust or move in response to a radially outward force above a threshold level that is acting on one or more of the bodies. The bodies may be pliable and/or made with a pliable material. The bodies may be interconnected via interconnecting regions. One or more of the bodies may be configured to articulate so as to conform to movement of a body tissue structure. A skeletal component may or may not extend through one or more of the plurality of bodies.