Abstract: A medical device may include an insertion device having a proximal end, a distal end, and a lumen extending therethrough. The medical device may further include a snare device configured to transition between a contracted state within the lumen of the insertion device, and an expanded state extending distally of the insertion device. The snare device may include a loop including a pair of legs and a distal tip. The distal tip may include a plurality of stabilizers between the pair of legs.

Abstract: An open-irrigated ablation catheter system includes a catheter body, and an electrode tip body mounted on a distal portion of the catheter body. The electrode tip body includes a proximal end configured for connection to the catheter body and a wall defining an open interior region and including one or more irrigation ports. The wall is conductive for delivering radio frequency (RF) energy. The catheter system further includes a proximal insert positioned partially within the catheter body and at least partially within the proximal end of the electrode tip body. The proximal insert includes a fluid inlet for receiving a cooling fluid delivered via the catheter body. The proximal insert forms a flow path configured to direct the cooling fluid from the fluid inlet to cool the distal portion of the catheter body and to cool a junction of the catheter body and the electrode tip body.

Abstract: A foldable antenna system particularly suitable for use in a radar system includes a first antenna and a second antenna providing signaling; a body part; at least an actuator connected to the body part; a first connection element; a second connection element configured to connect the second antenna to the first antenna; a third connection element movably connected to the first antenna and a carriage part fixing the actuator to a surface. One end of the first connection element is movably connected to the body part distal from the actuator and a second end is connected to the first antenna.

Abstract: Polypectomy devices and methods for making and using polypectomy devices are disclosed. An example polypectomy device may include an elongate sheath having a proximal end region and a distal end region. A shaft may be slidably disposed within the sheath. A handle may be coupled to the proximal end region of the sheath. The handle may be designed to axially shift the shaft relative to the sheath. A snare may be coupled to the shaft. The snare may include a first region, a traction region, and a distal tip region. The first region may have a non-circular cross-sectional shape. The traction region may include a plurality of traction members. At a position between two adjacent traction members the snare may have a reduced cross-sectional area relative to the first region. The distal tip region may have a circular cross-sectional shape.

Abstract: A medical device may include an insertion device having a proximal end, a distal end, and a lumen extending therethrough. The medical device may further include a snare device configured to transition between a contracted state within the lumen of the insertion device, and an expanded state extending distally of the insertion device. The snare device may include a loop including a pair of legs and a distal tip. The distal tip may include a plurality of stabilizers between the pair of legs.

Abstract: Polypectomy devices and methods for making and using polypectomy devices are disclosed. An example polypectomy device may include an elongate sheath having a proximal end region and a distal end region. A shaft may be slidably disposed within the sheath. A handle may be coupled to the proximal end region of the sheath. The handle may be designed to axially shift the shaft relative to the sheath. A snare may be coupled to the shaft. The snare may include a first region, a traction region, and a distal tip region. The first region may have a non-circular cross-sectional shape. The traction region may include a plurality of traction members. At a position between two adjacent traction members the snare may have a reduced cross-sectional area relative to the first region. The distal tip region may have a circular cross-sectional shape.

Abstract: A medical device may include an insertion device having a proximal end, a distal end, and a lumen extending therethrough. The medical device may further include a snare device configured to transition between a contracted state within the lumen of the insertion device, and an expanded state extending distally of the insertion device. The snare device may include a loop including a pair of legs and a distal tip. The distal tip may include a plurality of stabilizers between the pair of legs.

Abstract: A foldable antenna system particularly suitable for use in a radar system includes a first antenna and a second antenna providing signaling; a body part; at least an actuator connected to the body part; a first connection element; a second connection element configured to connect the second antenna to the first antenna; a third connection element movably connected to the first antenna and a carriage part fixing the actuator to a surface. One end of the first connection element is movably connected to the body part distal from the actuator and a second end is connected to the first antenna.

Abstract: A medical device may include an insertion device having a proximal end, a distal end, and a lumen extending therethrough. A snare device may be configured to transition between a retracted state within the lumen of the insertion device, and an extended state extending distally of the insertion device. The snare device may comprise a wire. A member may be disposed within the lumen of the insertion device. The member may be configured to maintain legs of the snare device in an open snare loop configuration in the extended state. In the open snare loop configuration, the wire may include an arcuate loop.

Abstract: An endoprosthesis includes a stent having an inner surface defining a lumen and an outer surface; and a polymeric cover on the outer surface of the stent. The polymeric cover includes a base and adhesion elements. When the endoprosthesis is expanded to the expanded state in a lumen defined by a vessel wall, the adhesion elements create an interlock between the vessel wall and the endoprosthesis.

Abstract: An open-irrigated ablation catheter system includes a catheter body, and an electrode tip body mounted on a distal portion of the catheter body. The electrode tip body includes a proximal end configured for connection to the catheter body and a wall defining an open interior region and including one or more irrigation ports. The wall is conductive for delivering radio frequency (RF) energy. The catheter system further includes a proximal insert positioned partially within the catheter body and at least partially within the proximal end of the electrode tip body. The proximal insert includes a fluid inlet for receiving a cooling fluid delivered via the catheter body. The proximal insert forms a flow path configured to direct the cooling fluid from the fluid inlet to cool the distal portion of the catheter body and to cool a junction of the catheter body and the electrode tip body.

Abstract: Polypectomy devices and methods for making and using polypectomy devices are disclosed. An example polypectomy device may include an elongate sheath having a proximal end region and a distal end region. A shaft may be slidably disposed within the sheath. A handle may be coupled to the proximal end region of the sheath. The handle may be designed to axially shift the shaft relative to the sheath. A snare may be coupled to the shaft. The snare may include a first region, a traction region, and a distal tip region. The first region may have a non-circular cross-sectional shape. The traction region may include a plurality of traction members. At a position between two adjacent traction members the snare may have a reduced cross-sectional area relative to the first region. The distal tip region may have a circular cross-sectional shape.

Abstract: A catheter adapted to measure a contact force. The catheter includes a proximal segment, a distal segment, and a spring segment. The spring segment extends from the proximal segment to the distal segment. The spring segment is configured to permit relative movement between the distal segment and the proximal segment in response to an application of the force on the distal segment. The spring segment includes a slotted tube having a longitudinal axis and a plurality of sensing elements. The sensing elements are disposed on surfaces of the slotted tube. The sensing elements are configured to output a plurality of signals indicative of the relative movement between the proximal segment and the distal segment.

Abstract: A medical device may include an insertion device having a proximal end, a distal end, and a lumen extending therethrough. A snare device may be configured to transition between a retracted state within the lumen of the insertion device, and an extended state extending distally of the insertion device. The snare device may comprise a wire. A member may be disposed within the lumen of the insertion device. The member may be configured to maintain legs of the snare device in an open snare loop configuration in the extended state. In the open snare loop configuration, the wire may include an arcuate loop.

Abstract: A medical device may include an insertion device having a proximal end, a distal end, and a lumen extending therethrough. The medical device may further include a snare device configured to transition between a contracted state within the lumen of the insertion device, and an expanded state extending distally of the insertion device. The snare device may include a loop including a pair of legs and a distal tip. The distal tip may include a plurality of stabilizers between the pair of legs.

Abstract: A transcatheter valve frame comprising a valve frame comprising an elongate tubular member having a longitudinal axis and a circumference, the elongate tubular member comprising a plurality of struts interconnected by peaks and valleys that define a closed cell construction comprising a plurality of interconnected cells, the valve frame is formed from a single piece of material comprising a metal or metal alloy, the valve frame having a diameter that increases upon axial compression and the valve frame comprising a locking mechanism integral with the valve frame configured to fix the diameter of the valve frame.

Abstract: An endoprosthesis includes a stent having an inner surface defining a lumen and an outer surface; and a polymeric cover on the outer surface of the stent. The polymeric cover includes a base and adhesion elements. When the endoprosthesis is expanded to the expanded state in a lumen defined by a vessel wall, the adhesion elements create an interlock between the vessel wall and the endoprosthesis.

Abstract: System and methods for adhering a patch of stimulation electrode(s) to blood vessels to stimulate a target site on the blood vessel are described. In various embodiments, the system includes an adhesion patch and at least one electrode. The adhesion patch includes a passive adhesion mechanism that may produce an adhesive force sufficiently strong to adhere the adhesion patch to the exterior of the blood vessel and to operationally position the at least one electrode for use in electrically stimulating a target site of the blood vessel. The adhesion patch may also include a release mechanism that is configured for a user to disengage the patch from the exterior of the blood vessel without significant trauma to the blood vessel. After being released, the adhesion patch may be re-adhered to a different target site of the blood vessel and stimulate the different target site.

Abstract: System and methods for adhering a patch of stimulation electrode(s) to blood vessels to stimulate a target site on the blood vessel are described. In one embodiment, the system includes an adhesion patch and at least one electrode. The adhesion patch includes an active adhesion mechanism that may produce an adhesive force sufficiently strong to adhere the adhesion patch to the exterior of the blood vessel and to operationally position the at least one electrode for use in electrically stimulating a target site of the blood vessel. The adhesion patch may also include a release mechanism that is configured for a user to disengage the patch from the exterior of the blood vessel without significant trauma to the blood vessel. After being released, the adhesion patch may be re-adhered to a different target site of the blood vessel and stimulate the different target site.

Abstract: Various techniques are described for replacement heart valve implantation. In one example, a system includes a specialized conduction system tissue activation potential sensing device, configured for delivery to an intracardiac region, a specialized conduction system tissue activation detector circuit, configured to detect, using the sensing device, a specialized conduction system tissue activation potential, and a processor circuit, configured to use information about the detected specialized conduction system tissue activation potential to generate a heart valve placement indication.