An apparatus for decreasing the adverse effect of erectile dysfunction includes an elastic waist band. A plurality of magnets are disposed in a generally end to end orientation to provide a magnetic loop assembly. A cloth sleeve preferably surrounds the magnets. The waist band encircles a waist of the user. Opposite ends of the magnetic loop assembly are secured in a spaced-apart relationship to a front portion of the waist band and to form a loop that descends below the waist band. Opposite ends of an elastic thigh band are attached to a rear portion of the waist band. A center of the magnetic tube assembly is attached to a center of the thigh band. The male enhancement loop is worn for a period of time prior to intercourse to help to improve the quality (i.e., hardness) and duration of male erection during intercourse.

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.

A moldable wrist brace. The brace includes a pocket with a moldable insert disposed therein. The pocket and insert extend substantially the full length of the brace to maximize the length of the user's wrist supported thereby. A plurality of straps and buckles are provided for retaining the brace on the user's wrist and providing a desired compression thereon. The straps include locking tabs that once inserted through the buckles resist withdrawal of the straps therefrom. One-handed donning of the brace is thus simplified by retention of the straps in engagement with the buckles.

The invention relates to an implantable stomach prosthesis for surgically replacing or augmenting all or part of the antrum and/or pylorus of a stomach. The prosthesis controls the passage of food from the stomach to the small intestine. The prosthesis may be configured to churn ingested material and release it from the stomach through a prosthetic pyloric valve. At least one expandable member is arranged to be expanded to control the passage of food and/or to mimic the churning action of a patient's stomach. The prosthesis includes an outer support structure, a flexible inner member forming a conduit for the movement of material, and at least one expandable member located between the outer support structure and inner member. An implantable pump system is provided for inflating and deflating the expandable member(s).

A bariatric device and method of causing at least partial satiety in a recipient includes positioning a body in a recipient, the body having a wall defining a lumen, the wall configured to generally conform to the shape and size of the proximal cardiac portion of the stomach. Force is exerted with the wall on the proximal cardiac portion of the stomach in the absence of food thereby activating receptors located in the proximal cardiac portion of the stomach, thereby influencing a neurohormonal feedback mechanism of the recipient to cause at least partial satiety by augmenting fullness caused by food and simulating fullness in the absence of food.

A surgical cutting block according to an exemplary aspect of the present disclosure includes, among other things, a block body including a top surface having a first thickness that extends between a first surface and an opposing second surface of the block body and a capture disposed at the top surface. The capture includes a second thickness that is less than the first thickness of the top surface.

An automated orthotic device with a treatment regimen and a method for using an automated orthotic device with a treatment regimen to provide a plurality of prescribed tension settings. The orthotic device may comprise a body brace, a controller, a data storage means, and a communication means to address the problem of patients being required to visit the physician's office every time an adjustment must be made in the prescribed tension setting in their automated orthotic device. In one embodiment, a plurality of prescribed tension settings in the automated orthotic device are sorted so that as the patient's condition improves, the next prescribed tension setting in the treatment regimen may be applied. In another embodiment, the physician is allowed to edit or supplement a patient's treatment regimen remotely by connecting to the automated orthotic device over a network.

A suprapyloric anchor assembly includes an antral cap having at least three stabilizing members configured to reside in an antrum and engage tissue circumscribing a pyloric valve. A duodenal member is configured to reside at least partially in a duodenal bulb, and one or more tethers connect the antral cap to the duodenal member. The tether(s) is/are configured to allow passage of stomach contents through the pyloric valve. Optionally, one or more gastric balloon(s) may attached to the suprapyloric anchor and be inflated with the gastric cavity.

A method for performing a medical procedure may comprise advancing a first device through a first body lumen. A distal portion of the first device may include a magnet. The method may further comprise advancing a second device through a second body lumen. The second device may include a magnetic field sensor. The method may further comprise_receiving a signal from the magnetic field sensor. The signal may be indicative of a magnetic field measured by the magnetic field sensor. The method may further comprise, if the received signal matches a magnetic field of the magnet, identifying a position of the magnet.

The present invention includes a method for treating penile implant infections that uses a synthetic high-purity calcium sulfate mixed with antimicrobials, which is capable of providing prolonged exposure of antimicrobials to the infection site and capable of acting as an intracorporal filler preventing fibrosis and loss of phallic length. The technique is especially useful for high-risk patients, and provides another medium for which antimicrobial agents can be delivered to a surgical infection site while at the same time acting as a filler, preventing fibrosis, and loss of the space. The antimicrobial cast lasts 4-6 weeks, making timely re-implantation easier, and preventing intracorporal fibrosis and loss of phallic length.