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.

Delivery devices for a stented prosthetic heart valve. The delivery device includes a spindle, at least one cord, and a lateral control feature. The cord is tensioned to crimp the prosthesis to a compressed condition for delivery to a target site. Tension is lessened to allow the prosthesis to self-expand. In a tethered and expanded state in which the prosthesis has self-expanded and is connected to the spindle by the cord, the lateral control feature directs the spindle to a prescribed location relative to the prosthesis appropriate for a functional evaluation of the prosthesis. In some embodiments, the spindle is directed to a center of the prosthesis; in other embodiments, the spindle is held at a commissure of the prosthesis. The lateral control features of the present disclosure assume numerous forms.

This invention provides a method for determining breast implant geometric properties, engineering stresses, engineering strains and engineering moduli; directly and quickly, using a load frame apparatus. More generally the invention provides a method for determining geometric properties and engineering mechanical properties of any elastomeric device, using a load frame apparatus. Engineering stress and engineering strain properties of breast implants are critical to their safety and durability. The geometric properties of breast implants undergoing compression also relates to the shape stability of breast implants, which may also be related to clinical outcomes such as capsular contracture and other untoward outcomes involving a breast capsule, such as Anaplastic Large Cell Lymphoma (ALCL), double capsule formation, seroma formation and associated breast implant illness (BII).

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 method of forming an implant having a porous tissue ingrowth structure and a bearing support structure. The method includes depositing a first layer of a metal powder onto a substrate, scanning a laser beam over the powder so as to sinter the metal powder at predetermined locations, depositing at least one layer of the metal powder onto the first layer and repeating the scanning of the laser beam.

The present invention relates to a surgical instrument (1) for deploying a prosthesis (200) and includes a first layer and second layer assembled together so as to define an internal space accessible to said surgical instrument (1) by means of an opening provided in said first layer, said surgical instrument including at least one sheet (2) made of a flexible resilient material, said sheet continuously overlapping itself one or more times so as to define a plurality of levels forming a spiral (3). The invention also relates to a kit including such a surgical instrument and such a prosthesis.

An orthopedic device for implanting between adjacent vertebrae comprising: an arcuate balloon and a hardenable material within said balloon. In some embodiments, the balloon has a footprint that substantially corresponds to a perimeter of a vertebral endplate. An inflatable device is inserted through a cannula into an intervertebral space and oriented so that, upon expansion, a natural angle between vertebrae will be at least partially restored. At least one component selected from the group consisting of a load-bearing component and an osteobiologic component is directed into the inflatable device through a fluid communication means.

Porous biocompatible structures suitable for use as medical implants and methods for fabricating such structures are disclosed. The disclosed structures may be fabricated using rapid manufacturing techniques. The disclosed porous structures each have a plurality of struts and nodes where no more than two struts intersect one another to form a node. Further, the nodes can be straight, curved, and can include portions that are curved and/or straight. The struts and nodes can form cells that can be fused or sintered to at least one other cell to form a continuous reticulated structure for improved strength while providing the porosity needed for tissue and cell in-growth.

The present invention relates to a prosthesis (1) for repairing an inguinal hernia defect comprising:

a piece (2) of biocompatible material having a preformed three-dimensional shape, including: a first portion (3) forming a partial spherical cap surface (8) shaped and dimensioned so as to substantially conform to the shape of the anterior abdominal wall, a second portion (4) extending from an inferior edge of said first portion and forming a wavy-shaped wall (9), shaped and dimensioned so as to substantially conform to the shape of the psoas muscle,

characterized in that said piece (2) further comprises:

a third portion (5) forming an arched part (10) extending longitudinally in the inferior direction from a medial inferior corner (3a) of said first portion, said arched part extending radially substantially in the front direction, said third portion being intended to face the medial inferior area of the inguinal anatomy.

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).