Abstract: An anastomosis device providing increased functionality, reliability and safety through the use of designs addressing potential puncture of an inflation balloon being used to hold and approximate tissue. The anastomosis device can include bladder retention structures configured to engage and retain tissue without pointed or sharpened surfaces that can rupture the inflation balloon. The anastomosis device can include a reinforced or otherwise protected inflation balloon to resist puncturing by a bladder retention structure. The anastomosis device can include a catheter wall profile selected to physically prevent bladder retention structures from being forcibly bent back so as to avoid potential contact with and puncture of the inflation balloon. The anastomosis device can include a catheter funnel with an internal spring for preventing kinking of the catheter lumen while providing for flexibility and stretch of the funnel to absorb pulling or shock force which can rupture the inflation balloon.

Abstract: A surgical tool which comprises an elongated body having a proximal end and a distal end, first and second sets of tissue approximating structures having deployed and retracted positions relative to the elongated body, an actuating mechanism extending from the proximal end of the elongated body for independently deploying and retracting each of the first and second sets of tissue approximating structures, a drainage lumen extending from a drainage aperture at the distal end of the elongated body to the proximal end, a main balloon adjacent to the distal end of the elongated body, and a strap connector extending from the elongated body that is connectable with a stabilization strap.

Abstract: A surgical tool including an elongated body having a proximal end and a distal end, first and second sets of tissue approximating structures having deployed and retracted positions relative to the elongated body, an actuating mechanism at the proximal end of the elongated body for independently deploying and retracting each of the first and second sets of tissue approximating structures, and a drainage lumen extending from a drainage aperture at the distal end of the elongated body to the proximal end. The tool further includes a main balloon adjacent to the distal end of the elongated body, wherein the first set of tissue approximating structures has a different configuration than the second set of tissue approximating structures.

Abstract: The invention is directed to a medical device, particularly a penile prosthesis, that includes an implantable element and a reservoir. The implantable element is configured to be implanted within the pelvic region of a patient and is designed to be capable of inflation and deflation via fluid transfer to and from the element. The reservoir is coupled to the implantable element. The fluid is drawn from the reservoir for inflation of the implantable element and returned to the reservoir for the deflation. The reservoir is approximately one inch or less in depth. The minimal depth enables the fluid reservoir to be placed in front of the puborectalis muscle and behind the abdominal fascia without being seen on an external view of the patient.

Abstract: The anastomosis devices of the invention advantageously provide reinforcement structures or components that increase the strength and/or flexibility of the device. These features can be especially beneficial to protect the integrity of the installation of the device within a patient to facilitate the healing process. These features may provide resistance to tearing or ripping of the catheter body or sheath by the tissue approximating structures and/or may provide strength in other areas of the catheter body. The anastomosis devices of the invention may further include method and devices for placing markers on the anastomosis device to facilitate accurate placement of the device within the patient.

Abstract: A method and apparatus for cutting a braided wire stent to a predetermined length such that a ball or sphere is formed on the end of each cut wire of the stent. These spheres are advantageous in that they provide added comfort to the patient and also act against the other wires of the stent to prevent the stent from becoming unbraided during the process of collapsing and expanding the stent such as is done when the stent is being inserted into a patient. The apparatus releasably holds and precisely positions the wires while the spheres are being formed.

Abstract: A method and apparatus for cutting a braided wire stent to a predetermined length such that a ball or sphere is formed on the end of each cut wire of the stent. These spheres are advantageous in that they provide added comfort to the patient and also act against the other wires of the stent to prevent the stent from becoming unbraided during the process of collapsing and expanding the stent such as is done when the stent is being inserted into a patient. The apparatus releasably holds and precisely positions the wires while the spheres are being formed.

Abstract: A fluid reservoir for a penile implant device that includes a body portion having a sleeve from which a tube may extend. The body portion includes support structure positioned at an interior surface of the body portion near an orifice of the reservoir, which orifice leads to a fluid passage of the tube. The support structure may comprise a plurality of protrusions that are arranged around the orifice and that extend from a base portion of the body portion. The invention also relates to a method of manufacturing a fluid reservoir for a penile implant device, which includes positioning a tube in a mold and injection molding a reservoir body onto the tube. More particularly, the method may include providing a mold, positioning a tube in the mold, injecting material into the mold, curing the material, and opening the mold to remove the reservoir body and tube assembly.

Abstract: A removable stent system and method for extraction of a removable stent from a target site is disclosed. The removable stent includes a removable stent having a collapsible end and a collapsing element configured for coupling with a removal tool. The collapsing element can be configured as a lasso or can be movable between two positions when deployed at a target site in vivo. The removable stent overcomes disadvantages and limitations of previous types of stents as well as overcoming complications during or following stent deployment in vivo. The removable stent further includes features that increase its ease of use and reduce the maneuvering required of devices or tools used to remove the stent. This then decreases the amount of effort required by the physician, the procedure time, and the level of discomfort experienced by a patient during the procedure.