A protector assembly for protecting an injury and/or surgical wound includes a protector shell having a shell front side, a shell back side and shell circumferential edge where the protector shell has a size and shape that is larger than the injury and/or surgical wound and shaped to correspond to a portion of the body having the injury and/or surgical wound to thereby protect the injury and/or surgical wound from further injury. The protector assembly also includes a protector pad having a pad front side, a pad back side and a pad circumferential edge wherein the protector pad has a pad opening sized to circumscribe the injury and/or surgical wound, the pad front side being attached to the shell back side of the protector shell where the pad back side is between the injury and/or surgical wound and the protector shell.

A passive stent for retaining an organ in an expanded state configured to adhere and substantially conform to an external surface of the organ may include an inner layer, an outer layer, and a middle layer that is enclosed by the inner layer and the outer layer, comprising a plurality of components configured to interlock and maintain the organ in an expanded state upon application of a vacuum. A method for retaining an organ in an expanded state may include applying at least one force to the organ to place the organ in the expanded state; applying a passive stent to an external surface of the organ; and applying a vacuum to the passive stent sufficient to cause a plurality of components of at least one layer of the passive stent to interlock, where the at least one layer is configured to maintain the organ in the expanded state after interlocking.

A gynecological device that corrects a vaginal opening that is large or stretched out without requiring surgery. The stretchable gynecological device includes a main body having a front surface, a rear surface, a first end, a second end, a first edge, a second edge, and an adhesive on the rear surface of the main body. The gynecological device also includes at least two arms having a front surface, a rear surface, a first end, a second end, a first edge and a second edge that extend outwardly from the second edge of the main body. An adhesive is on the rear surface of the arms. To apply the gynecological device, the arms are firmly pressed down to the vaginal vestibule bilaterally, the main body is then pulled up above the clitoral hood and then applied and pressed down across the lower abdomen towards the anterior superior iliac spines.

A support assembly (100) for supporting a transverse incision site (420) of a user (101) includes an assembly body (106) and a first assembly arm (102). The assembly body (106) is configured to encircle an abdomen (107) and at least one leg (311) of the user (101). The assembly body (106) includes a pelvic support layer (214) that is configured to provide a transverse supportive force to the transverse incision site (420) of the user (101). The first assembly arm (102) is coupled to the pelvic support layer (214). The first assembly arm (102) extends anteriorly from the assembly body (106). The first assembly arm (102) is configured to extend from a groin region (109) of the user (101) and secure to the assembly body (106) to adjust the transverse supportive force to the transverse incision site (420) at the peri-pelvic area (421).

A chest wound seal for treating traumatic pneumothorax following a penetrating chest wound. The chest wound seal comprises a wound pad with an absorbent bottom surface and a nonporous top surface embedded with unidirectional valves that allow evacuation of air and fluid from the pleural cavity but prevents re-entry of air into the thorax. A central vacuum column mounted over at least one unidirectional valve. The chest wound seal further comprises a plurality of wound pad segments radiating from the central vacuum column, wherein each segment comprises at least one manual valve configured to create a separate sealed area against the skin surface to suit body types with different size and morphological features. The central vacuum column is adapted to be connected to a vacuum pump which enables evacuation of harmful air and fluid from the pleural cavity thereby reducing the shock induced by hypoxia and increasing patient survivability.

The present invention concerns an improved article of clothing for nursing, with features that enhance the user's ability to selectively and controllably expose one or both breasts while simultaneously presenting a more secure and stylish look, both when in use and when not in use. The invention allows for individual or dual breast access in a non-obvious form that can provide as much breast coverage as the mother feels comfortable with. When access to the breast is not in use, the clothing shows no signs of having specific nursing functionality. The invention can be applied to articles of clothing in many fashion design style forms. The invention is also able to optionally provide breast support via an internal brassier, and nipple protection via removable pads.

A skin adhesive member that helps a user maintain an appropriate posture while supporting muscles on the abdominal side. The skin adhesive member extends in a length direction and is adhered from an abdominal side to a back side across a side abdomen of the user, the skin adhesive member having a foundation portion, a first extension portion extending in the length direction from one end of the foundation portion and adhered to the back side, a second extension portion extending from another end of the foundation portion and adhered to the abdominal side, wherein the first extension portion includes at least a pair of belt portions.

A skin adhesive member that helps a user maintain an appropriate posture while supporting muscles on the abdominal side. The skin adhesive member extends in a length direction and is adhered from an abdominal side to a back side across a side abdomen of the user, the skin adhesive member having a foundation portion, a first extension portion extending in the length direction from one end of the foundation portion and adhered to the back side, a second extension portion extending from another end of the foundation portion and adhered to the abdominal side, wherein the first extension portion includes at least a pair of belt portions.

A pressure bandage comprising an elastic band having a first end comprising a pocket member and a second end that is removably attachable to the first end. An inflatable bladder is placed in the pocket member and provides a substantially uniform pressure over a wound area when the band is placed on a patient and the bladder is inflated. The bladder is connected to a tube element which is used to inflate the bladder to the desired pressure. The elastic band may include a shoulder strap and may wrap over a patient's shoulder, across the patient's chest, and under the patient's opposite arm. The bottom side of the elastic band (facing the patient) may be made of a soft, absorptive material, and the bottom side of the pocket member may include an expandable mesh.

A pressure bandage comprising an elastic band having a first end comprising a pocket member and a second end that is removably attachable to the first end. An inflatable bladder is placed in the pocket member and provides a substantially uniform pressure over a wound area when the band is placed on a patient and the bladder is inflated. The bladder is connected to a tube element which is used to inflate the bladder to the desired pressure. The elastic band may include a shoulder strap and may wrap over a patient's shoulder, across the patient's chest, and under the patient's opposite arm. The bottom side of the elastic band (facing the patient) may be made of a soft, absorptive material, and the bottom side of the pocket member may include an expandable mesh.