The present invention relates to a surgical method of treating a patient. The method involves cutting the patient’s skin and abdominal wall, dissecting an area of the patient’s intestine, cutting the patient’s intestine so as to form an intestinal wall of a reservoir, implanting at least a pump as part of a flow control device so as to permanently reside inside the patient’s body and to act on said intestinal wall so as to reduce the reservoir’s volume in order to empty intestinal contents from the reservoir to outside the patient’s body, and thereafter, permanently closing the abdominal wall and skin.

A method of manufacturing a bead assembly for a sphincter augmentation device includes initiating 3D printing of a unibody housing such that the unibody housing defines a first opening, a chamber, and a magnet chamber. The method further includes pausing the 3D printing process, inserting a magnet within the magnetic chamber, and then resuming 3D printing of the unibody housing to form a hermetic seal between the magnet chamber and an external surface of the unibody housing.

An apparatus includes a plurality of beads and a linking assembly joining the beads together. The beads include a housing defining a first opening, a second opening, and a chamber extending between the first opening and the second opening. A magnet is contained within the housing. The beads and the linking assembly are arranged in an annular arrangement and sized to form a loop around an anatomical structure in a patient. The loop may move between a contracted and expanded configuration. The loop is magnetically biased toward the contracted configuration by a magnetic bias of the beads. The linking assembly includes a first link element having an elongate body extending in the chamber of the first bead and a sealing element attached to the elongate body housed within the first opening of the first bead to thereby form a hermetic seal.

A system and method for collecting operation data associated with a medical apparatus including an internal device implanted in a subject and an external device that is magnetically-coupled to and drives the internal device. The medical apparatus may be monitored to obtain raw data associated with the operation of the medical apparatus and one or more calculations may be performed on the raw data, wherein the raw data and/or calculated values may be associated with voiding frequency and voiding volume of the subject. A report may be generated from the raw data and/or calculated values. In addition, one or more signals may be sent to the external device and/or a docking station, or communicated by other means, to indicate to the subject that the operation of the medical apparatus should be altered.

A system includes an adjustable implant configured for implantation internally within a subject and includes a permanent magnet configured for rotation about an axis of rotation, the permanent magnet operatively coupled to a drive transmission configured to alter a dimension of the adjustable implant. The system includes an external adjustment device configured for placement on or adjacent to the skin of the subject having at least one magnet configured for rotation, the external adjustment device further comprising a motor configured to rotate the at least one magnet and an encoder. Rotation of the at least one magnet of the external adjustment device effectuates rotational movement of the permanent magnet of the adjustable implant and alters the dimension of the adjustable implant. Drive control circuitry is configured to receive an input signal from the encoder.

A medical device has an artificial contractile structure including at least one contractile element adapted to contract a hollow body organ in such a way that said contractile element is adapted to be in a resting position or in an activated position, the activated position being defined with the contractile element constricting the hollow body organ and the resting position being defined with the contractile element not constricting the hollow body organ. The medical device further includes a tensioning device adapted to apply a force so as to tighten the contractile element around the hollow body organ, the tensioning device having a flexible transmission with a tensioning element arranged in a sheath. The sheath has an inner coiled wire coiled in a first direction, and an outer coiled wire surrounding the inner coiled wire and coiled in a second direction opposite to said first direction.

Systems and methods are provided and adapted to engage and pull (e.g., pull up) or reposition urethral support tissue, such as the portion of the perineal membrane above or below the urethra. The perineal membrane intersects the urethra and vagina at the midurethra or distal location and can thus be stabilized or controlled in a manner that helps restore continence.

A medical implant system for implantation in a patient to treat erectile dysfunction includes a first fluid path, an inflatable penile prosthesis cylinder, an electric pump, and implant controller, and an implantable power supply. The inflatable penile prosthesis cylinder is in fluid communication with the first fluid path and is configured for implantation in a corpus cavernosum of a patient. The electric pump is in fluid communication with the first fluid path. The implant controller is electrically coupled to the pump and is configured to activate the pump to drive a flow of fluid through the first fluid path and into the cylinder. The implantable power supply provides electrical power to the pump.

A device for wrapping around a bodily organ and preventing overexpansion thereof. The device comprises inner and outer surfaces with a pliant material located therebetween. The inner surface defines a passage and accommodates and reinforces a bodily organ. The bodily organ, following surgical implantation, extends through the passage and is surrounded by the device. The inner surface, in an uncompressed/slightly compressed state, defines a normal state which supports the bodily organ and permits flow of bodily material therethrough. As the bodily organ expands, due to the bodily material flowing therethrough, the inner surface and the pliant material are compressed and, in turn, correspondingly exert a collapsing force, against the outer wall of the bodily organ, which limits and opposes the expansion of the bodily organ and forces the outer wall of the bodily organ back toward its normal state which still permits flow of bodily material through the bodily organ.

The present invention relates to a method for implanting an implantable apparatus for obtaining urinary control and emptying of the urinary bladder, thereby preventing from or treating involuntary urinary retention. In general terms, the apparatus comprises an expandable member adapted to be implanted inside the urinary bladder of the patient for discharging urine, and a control device for controlling the volume of the expandable member. The control device is adapted to be connected to the expandable member through the wall of the urinary bladder.