Abstract: An implantable device for penile construction can comprise an anchor plate and at least one attachment member. The anchor plate can be configured to engage with a first portion of a pelvic bone of a patient. The anchor plate can comprise a prosthesis attachment interface configured to be coupled to a penile prosthesis, and at least one attachment member configured to attach to the anchor plate. The at least one attachment member can be configured to engage with a second portion of the pelvic bone of the patient. The engagement of the anchor plate with the first portion of the pelvic bone and the engagement of the attachment member with the second portion of the pelvic bone can couple the pelvic bone between the anchor plate and the at least one attachment member.

Abstract: According to an aspect, an implant includes an inflatable member and a pump assembly configured to facilitate a transfer of a fluid from the reservoir to the inflatable member. The inflatable member defining a lumen and including a structural member. The inflatable member includes a coating.

Abstract: According to an aspect, an implant includes an inflatable member and a pump assembly configured to facilitate a transfer of a fluid from the reservoir to the inflatable member. The inflatable member defining a lumen and including a structural member. The inflatable member includes a coating.

Abstract: An implantable device for penile construction can comprise an anchor plate and at least one attachment member. The anchor plate can be configured to engage with a first portion of a pelvic bone of a patient. The anchor plate can comprise a prosthesis attachment interface configured to be coupled to a penile prosthesis, and at least one attachment member configured to attach to the anchor plate. The at least one attachment member can be configured to engage with a second portion of the pelvic bone of the patient. The engagement of the anchor plate with the first portion of the pelvic bone and the engagement of the attachment member with the second portion of the pelvic bone can couple the pelvic bone between the anchor plate and the at least one attachment member.

Abstract: 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.

Abstract: According to an aspect, an implant including an inflatable member and a pump assembly configured to facilitate a transfer of a fluid from the reservoir to the inflatable member. The inflatable member defines a lumen and includes a structural member. At least a portion of the structural member is disposed within the lumen defined by the inflatable member. In some implementations, the implant includes a reservoir configured to hold fluid.

Abstract: According to an aspect, an implant includes an inflatable member and a pump assembly configured to facilitate a transfer of a fluid from the reservoir to the inflatable member. The inflatable member defining a lumen and including a structural member. The inflatable member includes a coating.

Abstract: According to an aspect, an implant including an inflatable member and a pump assembly configured to facilitate a transfer of a fluid from the reservoir to the inflatable member. The inflatable member defines a lumen and includes a structural member. At least a portion of the structural member is disposed within the lumen defined by the inflatable member. In some implementations, the implant includes a reservoir configured to hold fluid.

Abstract: Described are implants and tools for use in treating pelvic conditions such as incontinence, including urinary incontinence in a male or female, for example an incontinence sling and delivery system that can include a sling implant and delivery tool system, wherein the implant can include a mesh sling and one or more anchors provided at or extending from a portion of the sling to facilitate tissue fixation; the delivery tool system can include at least a tunneler having a lumen, and an insertion tool; and wherein useful methods can involve inserting the tunneler through an incision and into a pelvic region of a patient, connecting the insertion tool to the sling, and inserting the sling into the tunneler to place the sling to provide tissue support.

Abstract: Embodiments are directed to an implantable penile prosthesis cylinder comprising an outer tube member and an inner tube member. The outer tube member has a longitudinal axis. The inner tube member is contained within the outer tube member. The inner tube member includes a plurality of inflatable chamber sections each defined by an exterior wall facing the outer tube member and an interior wall. Inflation of the chamber sections expands a girth of the outer tube member.

Abstract: A urethral stent device comprising a mechanical valve system is provided. The urethral stent device can be delivered up through the urethra via a flexible delivery tool. The valve mechanism is adapted to open when exposed to a certain amount of intraluminal pressure and can remain open until a desired cessation of fluid flow is achieved.

Abstract: A needleless fluid injection system include a working shaft (14) with a proximal end and a distal end, an injection shaft with a proximal end and a distal end, and a tissue tensioning mechanism (40) positioned at the distal end of at least one of the working shaft and the injection shaft. Embodiments of the tissue tensioning mechanism can include one or more of multiple radially expanding arcuate members (44), a linearly compressible element (60) with first and second plates at opposite ends of the linearly compressible element, an arcuate member (70) having a first end engaged within the lumen of the injection shaft and a second end moveable relative to the first end, first and second wedges (90a, b) that are slideable relative to each other, an inflatable bladder (110) with a foam material within a body opening of the bladder, at least two electromagnetic coils (146,148), or an electroactive polymer portion (166).

Abstract: Embodiments are directed to an implantable penile prosthesis cylinder comprising an outer tube member and an inner tube member. The outer tube member has a longitudinal axis. The inner tube member is contained within the outer tube member. The inner tube member includes a plurality of inflatable chamber sections each defined by an exterior wall facing the outer tube member and an interior Inflation of the chamber sections expands a girth of the outer tube member.

Abstract: Described are implants and tools for use in treating pelvic conditions such as incontinence, including urinary incontinence in a male or female, for example an incontinence sling and delivery system that can include a sling implant and delivery tool system, wherein the implant can include a mesh sling and one or more anchors provided at or extending from a portion of the sling to facilitate tissue fixation; the delivery tool system can include at least a tunneler having a lumen, and an insertion tool; and wherein useful methods can involve inserting the tunneler through an incision and into a pelvic region of a patient, connecting the insertion tool to the sling, and inserting the sling into the tunneler to place the sling to provide tissue support.

Abstract: An anastomosis training device and related methods of use that provides medical professionals with real-time feedback of pulling force. The anastomosis training device can include a housing portion, a spring member, a proximal catheter portion and a distal catheter portion. The housing portion can include an external tubing member that slidingly retains an internal tubing element and the spring member. A proximal wire assembly attaches the spring member to a manipulation assembly and a distal wire assembly attaches the spring member to a retention member that allows the anastomosis training tool to be anchored to a suitable surface. As a user applies a pulling force to the manipulation assembly, the internal tubing member is slidably withdrawn from the external tubing member to expose a visible force scale that indicates the level of pulling force being applied by the user.

Abstract: A urethral stent device comprising a mechanical valve system is provided. The urethral stent device can be delivered up through the urethra via a flexible delivery tool. The valve mechanism is adapted to open when exposed to a certain amount of intraluminal pressure and can remain open until a desired cessation of fluid flow is achieved.

Abstract: A needleless fluid injection system include a working shaft (14) with a proximal end and a distal end, an injection shaft with a proximal end and a distal end, and a tissue tensioning mechanism (40) positioned at the distal end of at least one of the working shaft and the injection shaft. Embodiments of the tissue tensioning mechanism can include one or more of multiple radially expanding arcuate members (44), a linearly compressible element (60) with first and second plates at opposite ends of the linearly compressible element, an arcuate member (70) having a first end engaged within the lumen of the injection shaft and a second end moveable relative to the first end, first and second wedges (90a, b) that are slideable relative to each other, an inflatable bladder (110) with a foam material within a body opening of the bladder, at least two electromagnetic coils (146,148), or an electroactive polymer portion (166).

Abstract: An anastomosis training device and related methods of use that provides medical professionals with real-time feedback of pulling force. The anastomosis training device can include a housing portion, a spring member, a proximal catheter portion and a distal catheter portion. The housing portion can include an external tubing member that slidingly retains an internal tubing element and the spring member. A proximal wire assembly attaches the spring member to a manipulation assembly and a distal wire assembly attaches the spring member to a retention member that allows the anastomosis training tool to be anchored to a suitable surface. As a user applies a pulling force to the manipulation assembly, the internal tubing member is slidably withdrawn from the external tubing member to expose a visible force scale that indicates the level of pulling force being applied by the user.