The present invention relates to a medical cast having a dual structure. The present invention provides the medical cast comprising: a skin protector coming into contact with the affected area of a patient, woven by mixing and using at least two kinds of functional fibers in order to increase adhesive strength with the skin, and manufactured such that diamond-shaped mesh holes are formed in the shape of a meshed net; an inner supporting cast formed to cover the outer side of the skin protector and comprising an inside supporting cast for absorbing sweat or body waste between the casts, an inner ventilating channel for covering the outer surface of the inside supporting cast and improving air permeability, an adhesion enhancing part for increasing the elasticity of the cast, and an inner rigidity reinforcing part for providing primary rigidity for the medical cast; and an outer supporting cast formed to cover the outer side of the inner supporting cast, impregnated with a hardening solution having hydraulic properties, and comprising an outer ventilating channel formed along the circumference thereof, an adhesion enhancing part connected with the outer ventilating channel so as to provide predetermined elastic force, a cutter part provided on one surface of the outer side thereof for guiding the progressing direction of a cutter blade, and outer rigidity reinforcing parts formed on both sides of the cutter part so as to provide secondary rigidity for the medical cast.

A method of producing a custom medical device including a splint or brace for immobilization of a selected region of a patient's body part. The custom medical device is produced in accordance with the following operations: (a) production of a three-dimensional mold of a portion of the patient's body part including the selected region onto which the desired medical device is to be placed; (b) definition of a three-dimensional shape of the desired medical device covering the selected region; (c) generation of a two-dimensional template corresponding to the defined three-dimensional shape, and which corresponds to unfolding in a two-dimensional plane of the three-dimensional shape of the desired medical device; (d) production of at least one plate of moldable material in accordance with the two-dimensional template of the desired medical device; and (e) molding of the plate of moldable material onto the three-dimensional mold to shape the desired medical device.

The system invention describes a support and improved method of application and removal. The support, comprised of a network of flexible, non-porous, multi-lumen tubing interlaces at a plurality of junctions to form a lattice structure. Apertures designed to accommodate boney prominences also permit air or water to reach the skin underneath and encourage rapid fluid flow internally through the lattice. A hydrophobic, thermal-resistant, flowable padding layer is injected within a secondary lumen to the lattice structure, spanning its complete surface area. As a result, the breathability of the support is not affected by this padding layer because it mirrors the apertures of the lattice. At least one liquid is injected into the structure and configured to transform into a solid when acted on by an external mechanical stimulus.

A wrist-hand-finger orthosis (100, 200) comprises a splint (110, 210) comprising a supporting splint section (120, 220) extending over the MCP joints and at least a greater portion of the fingers. The supporting splint section (120, 220) has a dorsal main surface (126, 226) adapted to face the palmar side of the hand. A wrist and forearm splint section (130, 230) is connected to or integral with the supporting splint section (120, 220). Inflatable bladders (140, 240; 150, 250) are arranged on the dorsal main surface (126, 226) at a MCP portion (122, 22) and a phalanx portion (124, 224) of the supporting splint section (120, 220) to be aligned with the MCP joints of the hand and the phalanges of fingers, respectively. The orthosis (100, 200) is particularly useful for human subjects having suffered from neurological diseases or cerebrovascular accident (CVA).

An orthopedic brace and method of making the same includes a wrap member having a first and second layer. The first layer includes a first sheet and a second sheet in a laterally spaced apart relationship. Each sheet has an inner side edge and an inner panel portion which extends the length of the corresponding sheet along the corresponding inner side edge. The second layer has first and second side edges, a first overlay portion extending the length of the second layer adjacent the first side edge and overlapping the first sheet's panel portion, a second overlay portion extending the length of the second layer adjacent the second side edge and overlapping the second sheet's panel portion, and a center portion that bridges the overlay portions. The layers are stitched together along spaced apart sets of seams.

A hand support including a base component arranged for securing to at least a portion of a hand, an anchor element adjustably connected to the base component and arranged for grasping a thumb, and a counterforce device connecting to the base component and the anchor element. The counterforce device arranged to generate a counterforce in combination with or against the base component and anchor element. The hand support may be arranged to provide traction for an extended period to remedy complications of the hand and associated joints

A cold therapy dynamic hand splint system is disclosed. The hand splint system includes an electric pump, a sleeve, an inflatable bladder, a refrigeration device, and a fluid reservoir. The sleeve includes a fluid-tight cavity filled with a cold fluid pressurized by the pump, and is wrapped around the forearm of a user. The inflatable bladder has an expanded state where the bladder is charged with the fluid pressurized by the pump and chilled by the refrigeration device, and a collapsed state where the bladder is substantially empty. The bladder is small enough that a portion fits inside a palm of a contracted spastic hand while in the collapsed state, and large enough to press the spastic hand open when the bladder is in the expanded state. The fluid is maintained within a therapeutic temperature range, and is in fluidic communication with the sleeve and the bladder through the pump.

A hand support including a base component arranged for securing to at least a portion of a hand, an anchor element adjustably connected to the base component and arranged for grasping a thumb, and a counterforce device connecting to the base component and the anchor element. The counterforce device arranged to generate a counterforce in combination with or against the base component and anchor element. The hand support may be arranged to provide traction for an extended period to remedy complications of the hand and associated joints.

An external fixation device for fractured forearms and/or hands. The device includes an arm-shaped main body and a cavity. The main body includes: a forepart which corresponds to a hand of a patient, and a rear part which corresponds to a segment extending from the hand to an elbow joint of the patient. The main body includes a first edge and a second edge. The first edge of the main body is provided with a flexible cotton member, and a placket is connected to the outer side of the flexible cotton member. The second edge of the main body is provided with a plurality of elastic belts. The rear part of the main body includes an opening which is located at a position corresponding to the elbow joint of the patient and communicates with the filler cavity.

The system invention describes an support and improved method of application and removal. The support, comprised of a network of flexible, non-porous, multi-lumen tubing interlaces at a plurality of junctions to form a lattice structure. Apertures designed to accommodate boney prominences also permit air or water to reach the skin underneath and encourage rapid fluid flow internally through the lattice. A hydrophobic, thermal-resistant, flowable padding layer is injected within a secondary lumen to the lattice structure, spanning its complete surface area. As a result, the breathability of the support is not affected by this padding layer because it mirrors the apertures of the lattice. At least one liquid is injected into the structure and configured to transform into a solid when acted on by an external mechanical stimulus.