An implant can be used for the treatment of fat pad atrophy. The implant can be installed in the ball of the foot, the heel of the foot, the hands, or other areas. The implant can supplement or replace a patient's fat pads. In some instances, the implant can include an implant pad having a non-permeable external lining and an internal cavity enclosed by the external lining. The internal cavity can include a filler material. The implant can include features that resist rupture and/or migration.

A foot patch is described herein where the foot patch is configured for placement upon a sole of a foot for sustained delivery of one or more agents. The patch may generally comprise a distal patch body and an elongated proximal portion positioned to project from one end of the distal portion. A proximal patch body may also be included for placement upon a heel of the sole of the foot. The patches may be infused with one or more agents including CBD, arnica oil, and menthol for transdermal delivery into the sole when the patches are adhered to the sole for a period of time.

A compression garment for a neurological disorder includes a body portion and a pad. The body portion may be operable to wrap around a foot and the pad can attach to an inner surface of the body portion. The pad can include an outward protrusion and/or an inward recess. A guide sleeve may be dimensioned to wrap together with the body portion around the foot, the pad being disposable between the body portion and the guide sleeve. A first tensioning band may be attached onto to first and second locations of the body portion and be operable to secure opposing first and second portions of the inner surface of the body portion to secure the outward protrusion and/or recess of the pad against the abductor hallucis and flexor hallucis brevis muscles of the foot. The outward protrusion can include a receiver for the metatarsal head.

Disclosure herein are protective bandage and methods of use and manufacture thereof. The protective bandages can include first and second flexible films and a shear-reducing element. The first flexible film may form a contact layer having a first side opposite a second side. The second flexible film may form a dome attached to and extending over a portion of the first side of the contact layer. The dome may have a height at least partially defined by a side wall and a top portion of the second flexible film. The contact layer may extend beneath the dome and the top portion being freely movable along the first side of the contact layer through a distance related to the height. The shear-reducing element is located inside the hollow dome.

A foot wrap (10) has a generally non-stretchable, flexible binding (11), a generally stretchable panel (12) coupled to the binding, an expandable, rotatable bladder (14), and a support pad (16) coupled to the binding opposite the bladder (14). The binding has a central portion (19) straddled by a first wing (21), a second wing (22), and an elastic heel band (23). The bladder measures approximately 3 inches by 3 inches and is designed to increase in height approximately 1½ to 1¾ inches with its inflation.

A negative pressure wound treatment system comprising a bandage portion and a negative pressure portion. The bandage portion includes a dressing portion in contact with a wound and a sealing layer positioned in contact with the dressing portion. The sealing layer includes an adhesive creating a seal around the wound. The negative pressure portion is in fluid communication with the bandage portion and includes a first valve and a second valve. The first valve is in fluid communication with the bandage portion and the negative pressure portion. The second valve is in fluid communication with the negative pressure portion and the surrounding environment. The negative pressure wound treatment system is configured to provide negative pressure to an area sealed by the bandage portion upon the actuation of the negative pressure portion. The negative pressure portion is configured to be actuated by compressing the negative pressure portion while walking.

A supporting pair of socks for disorders caused by foot deformities is provided that can be worn on daily basis and it allows comforting of foot in case of flatfoot and hallux valgus disorder.

An elongate strap support system for anatomical support, pain reduction, or therapeutic treatment includes a package containing a first elongate strap support and at least one additional elongate strap support. In one example, the first elongate strap support includes a woven fabric support layer including synthetic fibers. The woven fabric is shaped so as to form an elongated strap with rounded portions. The woven fabric is substantially resistant to stretching in one direction under such test conditions as those specified in ASTM D3759. The first elongate strap support additionally includes an adhesive layer on the support layer for adhesive attachment of the woven fabric support layer to an outer skin surface of a body and a removable cover layer on the adhesive layer.

A method for manufacturing stretch resistant plantar fascia support system is provided. The stretch resistant plantar fascia support system is adhesively applied to the foot of a patient for providing relief from plantar fasciitis. A portion of the stretch resistant plantar fascia support system is adhesively attached to the bottom surface of the foot for reducing stress on the plantar fascia.

A negative pressure wound treatment system comprising a bandage portion and a negative pressure portion. The bandage portion includes a dressing portion in contact with a wound and a sealing layer positioned in contact with the dressing portion. The sealing layer includes an adhesive creating a seal around the wound. The negative pressure portion is in fluid communication with the bandage portion and includes a first valve and a second valve. The first valve is in fluid communication with the bandage portion and the negative pressure portion. The second valve is in fluid communication with the negative pressure portion and the surrounding environment. The negative pressure wound treatment system is configured to provide negative pressure to an area sealed by the bandage portion upon the actuation of the negative pressure portion. The negative pressure portion is configured to be actuated by compressing the negative pressure portion while walking.