The present invention relates to biologic tissues, which are used to create cellular matrix scaffolds to help repair the body. The invention discloses two specific implant shapes that are pre-cut to address two separate pelvic floor prolapses (anterior and/or posterior). Additionally, the method of providing surgeries-specific pre-shaped biologic scaffolds is also claimed.

The present invention relates to the diagnosis and treatment of pelvic floor prolapse. The diagnosis and treatment may involve the use of a multiple sensor-enabled device for vaginal insertion capable of providing real-time data regarding the pa -tient’s physiology, the position and movement of the urethra, and the muscular strength of the patient’s vagina and pelvic floor. The methods and devices of the invention may also be useful to addressing other medical issues, including urinary incontinence, sexual health, and fecal incontinence, as well as facilitate patient home wellness activities.

The present invention relates to apparatus for treating urinary incontinence in a patient. In the apparatus, there is at least one adjustable lifting device adapted to lift the urethra or neck of the urine bladder, thereby affecting the patient’s incontinence. The lifting device is provided with first and second fixation devices and an interconnecting part extending uninterruptedly between the first and second fixation devices.

The invention provides an implantable system for managing urinary incontinence. The system includes a sling with an elongate body member having a proximal portion, a distal portion and an intermediate portion. The intermediate portion is configured to be positioned underneath urethra of a subject for providing an adequate support to prevent leakage of urine during a stress event. The system may include a pressure sensor communicatively coupled with the elongated body member and configured to be positioned in an abdominal cavity and adapted to sense an increase in intra-abdominal pressure. The pressure sensor generates a first signal that is indicative of a change in the intra-abdominal pressure upon occurrence of the stress event. The system includes a processing circuit to process the first signal sensed by the pressure sensor. The processing circuit is configured to generate a second signal causing an adjustment of tensioning force in the elongate body member thereby changing magnitude of a supporting force to the urethra.

According to an example aspect of the present invention, there is provided an auxetic structure, comprising or consisting of cellulosic material, preferably comprising nanostructured or microstructured cellulose on at least one of its surfaces or consisting of nanostructured or microstructured cellulose and optionally other cellulosic material.

A T-shaped anchorable mesh having a reticular structure with an intertwining mesh material, forming a tissue contact surface. The T-shaped anchorable mesh includes a long arm and a fixation part. The long arm has two lateral ends spaced from each other in an X direction and two marginal edges extending between the two lateral ends. The fixation part extends from one of the two marginal edges in a Y direction. The fixation part includes a plurality of protrusions emerging from the tissue contact surface.

One or more sensors are incorporated onto one or more of an implantable device and a surgical tool used for placement and/or adjustment of the implantable device. The implantable device includes an adjustable membrane element for controllable coaptation of a body lumen, such as coaptation of a urethra as treatment for urinary incontinence. In various embodiments, the one or more sensors can be configured to detect information indicative of at least one of a shape of the adjustable membrane element, a position of the adjustable membrane element relative to the body lumen, or a shape of the body lumen.

A sling assembly for treatment of stress urinary incontinence may comprise a midline marker, a sling, and a sleeve. The midline marker identifies the midpoint of the protective sleeve when it is installed on a transparent surface of the sleeve. The protective sleeve comprises a clear transparent surface and a colored opaque surface. During a procedure, the colored opaque surface of the sleeve provides contrast between the surfaces of the sleeve to identify any twisting present throughout the length of the sleeve. The clear transparent surface of the sleeve forms a channel at the center of the midline marker when the transparent surface of the sleeve is wrapped over the body of the midline marker. The channel is large enough for a surgical instrument to be inserted and cut the transparent surface to separate the sleeve from the midline marker after installation of the sling at a desired location.

A method of attaching a surgical suture inside of a pelvis includes moving an anchor deployment component relative to the anchor delivery component, pushing an anchor out of the anchor delivery component and into tissue inside of the pelvis, and engaging anchor with the tissue inside of the pelvis.

A method of treating prolapse of a vagina includes supporting the vagina by implanting a sacrocolpopexy support and locating an exterior surface of the vagina between leg portions of a vaginal cuff section of the support, and securing a head section of the support to a ligament or a sacrum while isolating the head section from contact with tissue of the vagina.