Abstract: Medical devices for cinching and cutting one or more suture, and methods for making and using such devices are disclosed. An example medical device may include a shaft, a sleeve attached to the shaft, cutter slidable within the sleeve, a cinch sleeve releasably coupled to the sleeve, and a cinch member. An elongated inner shaft may extend through and be longitudinally movable within the elongated shaft, sleeve, cutter, cinch sleeve, and cinch member. The inner shaft may be actuated to cinch and cut one or more suture disposed within the device.

Abstract: A tubular prosthesis that includes a scaffolding formed by at least one scaffolding filament; a cover; and at least one controlled ingrowth feature constructed and arranged to abut an inner surface of a lumen wall when the prosthesis is implanted in the body lumen. The controlled ingrowth feature may extend inwards or outwards from the prosthesis outer surface.

Abstract: A tubular prosthesis that includes a scaffolding formed by at least one scaffolding filament; a cover; and at least one controlled ingrowth feature constructed and arranged to abut an inner surface of a lumen wall when the prosthesis is implanted in the body lumen. The controlled ingrowth feature may extend inwards or outwards from the prosthesis outer surface. The controlled ingrowth feature may be formed by a scaffolding filament; by a separate filament; by the cover; and combinations thereof.

Abstract: A method of loading an expandable stent into a delivery device may include positioning a middle portion of the expandable stent in a collapsing fixture including a passage extending therethrough, radially compressing the middle portion of the expandable stent in the passage before any other portion of the expandable stent while a first end of the expandable stent is disposed outside of the passage, moving the collapsing fixture relative to the expandable stent, radially compressing the expandable stent from the middle portion toward the first end of the expandable stent, and inserting the first end of the expandable stent followed by the middle portion of the expandable stent into a distal end of an elongate outer sheath of the delivery device.

Abstract: A tubular prosthesis that includes a scaffolding formed by at least one scaffolding filament; a cover; and at least one controlled ingrowth feature constructed and arranged to abut an inner surface of a lumen wall when the prosthesis is implanted in the body lumen. The controlled ingrowth feature may extend inwards or outwards from the prosthesis outer surface. The controlled ingrowth feature may be formed by a scaffolding filament; by a separate filament; by the cover; and combinations thereof.

Abstract: A tubular prosthesis that includes a scaffolding formed by at least one scaffolding filament; a cover; and at least one controlled ingrowth feature constructed and arranged to abut an inner surface of a lumen wall when the prosthesis is implanted in the body lumen. The controlled ingrowth feature may extend inwards or outwards from the prosthesis outer surface. The controlled ingrowth feature may be formed by a scaffolding filament; by a separate filament; by the cover; and combinations thereof.

Abstract: A method of loading an expandable stent into a delivery device may include positioning a middle portion of the expandable stent in a collapsing fixture including a passage extending therethrough, radially compressing the middle portion of the expandable stent in the passage before any other portion of the expandable stent while a first end of the expandable stent is disposed outside of the passage, moving the collapsing fixture relative to the expandable stent, radially compressing the expandable stent from the middle portion toward the first end of the expandable stent, and inserting the first end of the expandable stent followed by the middle portion of the expandable stent into a distal end of an elongate outer sheath of the delivery device.

Abstract: A tubular prosthesis that includes a scaffolding formed by at least one scaffolding filament; a cover; and at least one controlled ingrowth feature constructed and arranged to abut an inner surface of a lumen wall when the prosthesis is implanted in the body lumen. The controlled ingrowth feature may extend inwards or outwards from the prosthesis outer surface. The controlled ingrowth feature may be formed by a scaffolding filament; by a separate filament; by the cover; and combinations thereof.

Abstract: A gastrostomy device includes an elongate tube extending from a proximal end to a distal end and having a tube diameter. The elongate tube has a length that enables the elongate tube to extend from a position exterior a patient to a position interior the patient's stomach. A resealable valve is disposed within the proximal end of the elongate tube. An inflation lumen extends along the elongate tube and an inflation port is disposed near the proximal end of the elongate tube and is in fluid communication with the inflation lumen. A silicone balloon is secured relative to the distal end of the elongate tube and is in fluid communication with the inflation lumen. The silicone balloon has a distal region, a proximal region and an intervening middle region that, when inflated, stretches more than the distal region or the proximal region.