A patellofemoral support comprises a sleeve and a strap assembly. The strap assembly is arranged to extend helically about the sleeve. A buttress is arranged to removably secure to an inside surface of a first portion of the strap assembly or to the sleeve.

A patellofemoral support comprises a sleeve and a strap assembly. The strap assembly is arranged to extend helically about the sleeve. A buttress is arranged to removably secure to an inside surface of a first portion of the strap assembly or to the sleeve.

An aural hematoma splint (AHS) system/method providing for animal ear pinna (AEP) suspension and/or compression allowing non-surgical treatment of AEP auricular hematoma is disclosed. The AHS promotes healing performance by including a conical primary plate (CPP) and angular secondary plate (ASP) that are used in conjunction with non-elastic fabric tape (NFT) to hold the AEP in suspension during treatment. The NFT includes a long strap collar (LSC) and cross support strips (CSS) for preparatory taping and application of the CPP/ASP to the AEP. This sandwich configuration of the CPP/ASP surrounding the AEP creates equilibrium in hematoma fluid pressures within the damaged area of the AEP, promotes a uniform thin layer of blood to clot in the entirety of the hematoma region, and allows regeneration of damaged tissues in a controlled environment while limiting structural and aesthetic damage to the healed AEP post treatment.

An aural hematoma splint (AHS) system/method providing for animal ear pinna (AEP) suspension and/or compression allowing non-surgical treatment of AEP auricular hematoma is disclosed. The AHS promotes healing performance by including a conical primary plate (CPP) and angular secondary plate (ASP) that are used in conjunction with non-elastic fabric tape (NFT) to hold the AEP in suspension during treatment. The NFT includes a long strap collar (LSC) and cross support strips (CSS) for preparatory taping and application of the CPP/ASP to the AEP. This sandwich configuration of the CPP/ASP surrounding the AEP creates equilibrium in hematoma fluid pressures within the damaged area of the AEP, promotes a uniform thin layer of blood to clot in the entirety of the hematoma region, and allows regeneration of damaged tissues in a controlled environment while limiting structural and aesthetic damage to the healed AEP post treatment.

A pelvic prolapse treatment belt may include a main structural member having an inner and outer layer. The main structural member may include a plurality of through-hole regions positioned to be located on respective sides of a wearer's spine and a single through hole positioned at an approximate center of a rear of the main structural member. A compression pad may be attached to the main structural member. The compression pad may be configured for placing over a pelvic cavity of the wearer. A single strap may be attached to a bottom end of the compression pad and have a length sufficient for extending over the wearer's intergluteal cleft. The single strap may be sized for inserted through the single through-hole and have a distal end attached to a waist strap. The waist strap may include attachment features for attaching to the outer side of the main structural member.

A pelvic prolapse treatment belt may include a main structural member having an inner and outer layer. The main structural member may include a plurality of through-hole regions positioned to be located on respective sides of a wearer's spine and a single through hole positioned at an approximate center of a rear of the main structural member. A compression pad may be attached to the main structural member. The compression pad may be configured for placing over a pelvic cavity of the wearer. A single strap may be attached to a bottom end of the compression pad and have a length sufficient for extending over the wearer's intergluteal cleft. The single strap may be sized for inserted through the single through-hole and have a distal end attached to a waist strap. The waist strap may include attachment features for attaching to the outer side of the main structural member.

A garment for providing orthopedic support or therapy to a human body may include a tubular flexible element and a tension strap. The tubular flexible element may be disposed around at least some portion of a human body and include flexible and a touch fastener portions. The flexible portion may be at an exterior of the tubular flexible element and cover a first portion of the body. The touch fastener portion may be at the exterior of the tubular flexible element and cover a second portion of the body. The tension strap may include first and second ends, where the first end includes a first touch fastener to be coupled with the touch fastener portion at a first location, and the second end includes a second touch fastener to be coupled with the touch fastener portion at a second location, thereby applying tension between the first and second locations.

A garment for providing orthopedic support or therapy to a human body may include a tubular flexible element and a tension strap. The tubular flexible element may be disposed around at least some portion of a human body and include flexible and a touch fastener portions. The flexible portion may be at an exterior of the tubular flexible element and cover a first portion of the body. The touch fastener portion may be at the exterior of the tubular flexible element and cover a second portion of the body. The tension strap may include first and second ends, where the first end includes a first touch fastener to be coupled with the touch fastener portion at a first location, and the second end includes a second touch fastener to be coupled with the touch fastener portion at a second location, thereby applying tension between the first and second locations.

A use of an umbilical splint for shaping an umbilicus after an abdominal operation is described. The umbilical splint may comprise an insertion portion extending in a longitudinal direction and terminating at an insertion end for insertion into the umbilicus. Furthermore, the insertion portion may comprise a bulbous section near the insertion end. The bulbous section may be operable to apply pressure to a tissue of the umbilicus after the abdominal operation. The insertion portion may have different cross-sectional shapes including circular and oval. Finally, the insertion portion may be configured to engage the umbilicus such that the umbilical splint is retained within the umbilicus.

A use of an umbilical splint for shaping an umbilicus after an abdominal operation is described. The umbilical splint may comprise an insertion portion extending in a longitudinal direction and terminating at an insertion end for insertion into the umbilicus. Furthermore, the insertion portion may comprise a bulbous section near the insertion end. The bulbous section may be operable to apply pressure to a tissue of the umbilicus after the abdominal operation. The insertion portion may have different cross-sectional shapes including circular and oval. Finally, the insertion portion may be configured to engage the umbilicus such that the umbilical splint is retained within the umbilicus.