According to an aspect, an implantable device for penile construction includes an anchor plate configured to be coupled to a pelvic bone of a patient, where the anchor plate has an attachment interface configured to be coupled to a penile prosthesis after the anchor plate is coupled to the pelvic bone.

According to an aspect, an implantable device for penile construction includes a penile implant having a distal portion and a proximal portion. The distal portion includes a shaft portion configured to be disposed in a neophallus. The proximal portion defines a first strut and a second strut, and the proximal portion is configured to be attached to a pelvis structure.

A system for managing female incontinence includes a body of biocompatible material configured to fit between the labia minora and the vestibule floor, the body having a surface configured to occlude the urethral meatus, a first adhesive layer disposed on at least a first portion of the surface and configured to provide a sealing engagement between the body and the urethral meatus, and a second adhesive layer disposed over the first adhesive layer and configured to provide a sealing engagement between the body and the urethral meatus, wherein the second adhesive layer is removable from the first adhesive layer.

An embodiment includes a penile prosthetic comprising: an expandable conduit; a pump; a reservoir; a first conduit that couples the expandable conduit to the pump; a second conduit that couples the reservoir to the pump; and a plate that couples to the expandable conduit, wherein the plate includes a concave surface. Other embodiments are described herein.

A system for managing female incontinence includes a body of biocompatible material configured to fit between the labia minora and the vestibule floor, the body having a surface configured to occlude the urethral meatus, an adhesive carried on at least a first portion of the surface and configured to provide a sealing engagement between the body and the urethral meatus, and a substance carried by at least one of the body and the adhesive and configured for controlling the odor of the general vaginal-urethral area of a female.

A hybrid medical device that can aid in reconstructive or augmentative surgery of the breast is disclosed. The device can utilize a suitable biological collagen tissue matrix combined with a synthetic material, for example, that can impart a high initial strength to the repair site while permitting proper healing and revitalization of the implanted device.

The present disclosure provides a system of gender specific pharmaceuticals. The system includes a first package of a pharmaceutical for use by a male and a second package of a pharmaceutical for use by a female. The first package includes a pharmaceutical for use by a male and a first label coupled to the first package, wherein at least one of the first package and first label includes a male specifier and a recommended male dosage. The second package includes a pharmaceutical for use by a female and a second label coupled to the second package, wherein at least one of the second package and second label includes a female specifier and a recommended female dosage.

A comfortable single-piece male incontinence control device (100) permitting conscious micturition without adjustment or removal of the device (100). The device having a continuous loop of an elastic compression band (110) configured and arranged to securely encircle a flaccid penis P without inflicting penile ischemia, and a bump (120) on the elastic compression band (110) projecting inward into the lumen (119) defined by the band (110) for pressing against and constricting the urethra U of a wearer W.

A breast prosthesis comprises a resiliently-compliant silicone shell (1;11) which has an outer wall (2;12) configured to simulate the shape of a female breast. The wall (2;12) is fretted with an ornamental pattern of perforations (6;16) that vent the internal cavity (4;14) of the shell (1;11), and ribs (5;15) within the cavity (4;14) extend across it in resiliently supporting and retaining the breast-shape of the shell (1;11). The ribs (5;15) are interconnected with one another and are molded integrally with the outer wall (2;12). The shell (1:11) has a flat peripheral rim (3:13) to the cavity (4:14).

The disclosure describes a breast implant device product that mimics the natural pectoral fat of the breast and is characterized by an incomplete pyramid with isosceles triangular base and wedge-shaped edges and sloping faces that meet at acute angles with variable degree located medially, laterally, and on the top and a footprint characterized by a semicircular lower portion and an oval paraboloid upper portion and a center of gravity located closer to the footprint than to the profile, the said footprint is advantageously converging and moving towards the underlying surface as the chest wall with a method of manufacturing and a method of use of the said implant including a breast pyramid sizing system.