Disclosed is a biocompatible hemostatic nose clip having an interconnected body, arms and hands, which is intended for use in nosebleeds (epistaxis) that originate from the nasal septum, and is suitable for the personal use of children or adults without the need for medical personnel. The nose clip is insertable or removable with one hand.

A device for treating a tissue opening includes a proximal portion including an elongated flexible member, a capsule releasably coupled to a distal end of the flexible member and including a lumen extending therethrough and a clip including a pair of arms movably housed within the capsule. A suture extending along a first one of the pair of arms and including a loop at a distal end thereof extending across an opening extending through the first one of the pair of arms. A suture grabbing element extending laterally from a second one of the pair of arms and including a hook so that, when the pair of arms are moved toward a closed configuration, the hook extends through the opening to grab the loop and draw the distal end of the suture from the first one of the pair of arms toward the second one of the pair of arms.

Clip for an aneurism suitable for being implanted into tissue in which an aneurism has formed and carrying out a tight closure of the aneurism which comprises a pair of claw members (2a, 2b) made of non-metallic material, said claw members being provided with articulated joining means (3) which allow the rotation of the pair of claw members around a pivot (4) which interlocks them, the clip being able to adopt at least one opening position (A) and one closure position (B); the clip being provided with at least one spring element (6) at least partially housed in the clip which bends to arrange the clip in closure position which comprises at least one flexible (7) and elastic element with a section with arced configuration (8), press-fitted with two opposing ends (9a, 9b) each one exerting pressure on a different claw member both in the opening and in the closure position.

In a preferred embodiment of the present invention, a surgical brace device for deployment across a line of stapled tissue of an organ comprises: a first splint member and a second splint member having a first end and a second end, and configured to be disposed on either side of the surgically stapled tissue; at least one strut member having a first end and a second end, wherein said first end of the strut member is fixedly joined with said first end of said first splint member and said second end of the strut member is fixedly joined with said first end of said second splint member and wherein said first splint member and said second splint member is dimensioned to span at least a portion of the width of said line of stapled tissue and a predetermined portion of said undisturbed tissue of said organ adjacent thereto; and a tie member configured to traverse the tissue of said organ disposed at a predetermined distance from said at least one strut member to interconnect and keep said first splint member and said second splint member from spreading and anchor said surgical brace device to said organ.

Embodiments of a leaflet clip device and method of reducing regurgitation through a native heart valve are disclosed. A leaflet clip device can include an elongated clipping member having a first end portion and a second end portion and a tensioning mechanism coupled to the clipping member. The leaflet clip device can further include one or more tensioning members disposed within a lumen of the clipping member, wherein the one or more tensioning members are operatively connected to the tensioning mechanism to transform the clipping member from a delivery configuration to an implantation configuration.

A prosthetic device for sealing a native heart valves to prevent or reduce regurgitation comprises a spacer having one or more anchors. The spacer may also have atrial support structures, ventricular support structures, or both atrial and ventricular support structures In some cases, the spacer has anchors that attach to the leaflets as well as atrial and ventricular support. In some cases, the spacer straddles the annulus and is located by anchors, and in some cases the support structures can be implanted within the native heart valve. In some cases, the prosthetic device reduces the annulus diameter when implanted within the native heart vasculature. In some cases, the prosthetic device cinches the annulus when implanted within the native heart vasculature.

The present disclosure relates generally to the field of medical devices for clamping a leaflet of a heart valve. In particular, the present disclosure relates to medical devices, systems, and methods for delivering artificial chordae tendineae in a patient. In an embodiment, a system may include a clamp having a plurality of arms at a first end. The plurality of arms may have a closed configuration in which the arms are oriented toward each other, and an open configuration in which the arms are oriented away from each other. A spring portion may be coupled to the plurality of arms at a second end that is configured to bias the arms to the closed configuration. The arms of the clamp may be configured to fixedly engage with a leaflet of the heart valve. The second end of the clamp may be configured to couple to an artificial chordae tendineae.

The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to traction systems, and methods of use thereof, for endoscopic procedures such as tissue dissection. For example, a traction system may include a filament extendable along an outer surface of an endoscope with a distal end of the filament attachable to a medical device engaged with a target tissue of a body lumen.

A medical implant (20) includes first and second ring members (22, 24), each including a resilient framework (26) having a generally cylindrical form. A tubular sleeve (28) is fixed to the first and second ring members so as to hold the ring members in mutual longitudinal alignment, thereby defining a lumen (32) passing through the ring members. A constricting element (30) is fit around the sleeve at a location intermediate the first and second ring members so as to reduce a diameter of the lumen at the location.