An exemplary valve repair device for repairing a native valve of a patient includes: a coaption element formed from a strip of material; a pair of extension members; a pair of paddles formed from the strip of material and connected to the coaption element; and a cap attached to the paddles. The paddles are movable between an open position and a closed position, are disposed over the extension member, and are configured to attach to the native valve of the patient. Movement of the cap toward the coaption element causes the pair of paddles to move to the closed position, and movement of the cap away from the coaption element causes the pair of paddles to move to the open position. The cap has a retention body for receiving attachment portions of the extension members, a retaining nut, and a retaining bolt for securing the retaining nut.

Vascular filters and deflectors and methods for filtering bodily fluids. A blood filtering assembly can capture embolic material dislodged or generated during an endovascular procedure to inhibit or prevent the material from entering the cerebral vasculature. A blood deflecting assembly can deflect embolic material dislodged or generated during an endovascular procedure to inhibit or prevent the material from entering the cerebral vasculature.

Various temporary or removable valve devices having an expandable frame comprising a flexible material and a membrane attached to the expandable frame, wherein the temporary valve device is movable into an expanded configuration for deployment of the device in a target vascular area and further is movable into a collapsed configuration for both delivery of the device to the target vascular area and for removal of the device from the target vascular area.

An implantable prosthetic device includes a plurality of anchor members, a plurality of clasps, and a cover. The plurality of clasps are configured to capture the leaflets to secure the leaflets to the anchor members. The cover is disposed over the plurality of anchor members. The cover can also be disposed over the clasps and a spacer member. A portion of the cover can be covered by a coupler. One or more extensions of a coupling collar can extend through the cover.

The present disclosure discloses a swimming earplug, which comprises an ear cap and a bracket, wherein the ear cap is a soft rubber ear cap, an ear cap through hole is provided at the center of the ear cap, the ear cap through hole penetrates the front and rear ends of the ear cap, an insertion post is formed at the front end of the bracket, the insertion post is inserted into the ear cap through hole and snugly fitted with the ear cap through hole, a bracket, through hole is provided in the bracket, the front end of the bracket through hole extends to a front end face of the insertion post such that the bracket through hole and the ear cap through hole communicate with each other, a rear end opening of the bracket through hole is covered with a waterproof and breathable membrane, and the waterproof and breathable membrane is fixedly connected to the bracket. Through the present disclosure, it is possible to effectively prevent water from entering an ear, the wearing comfort is better, and outside sounds can be heard clearly.

The inventions relates to a transurethral catheter device for bleeding control in pelvic fractures. The catheter device comprises an expandable body assembly with at least one expandable body. The expandable body assembly comprises a proximal portion, a center portion and a distal portion. The expandable body assembly is configured to be expanded from a collapsed state to an expanded state by expanding the at least one expandable body. The expandable body assembly is further configured to be inserted into the urinary bladder of a patient via the urethra in the collapsed state. In the expanded state, the proximal portion has a length l.sub.1 and a width w.sub.1, the center portion a length l.sub.2 and a width w.sub.2, the distal portion a length l.sub.3 and a width w.sub.3, and the expandable body assembly a total length l. A displacement volume V of the expandable body assembly in the expanded state is larger than 0.5 liters. The width w.sub.2 is smaller than 50% of the width w.sub.3. The width w.sub.1 is larger than a width {tilde over (w)}.sub.1 of the proximal portion in the collapsed state and the width w.sub.3 is larger than a width {tilde over (w)}.sub.3 of the distal portion in the collapsed state. The length l.sub.1 is smaller than 25% of the total length l. This allows for arranging the expandable body assembly in the expanded state in the urinary bladder such that the proximal portion is adjacent to the internal urethral orifice of the urinary bladder and the center portion is adjacent to the ureter orifices of the urinary bladder, but not in contact with the ureter orifices.

The application provides a valve clamping system. The valve clamping system includes a pushing device and a valve clip with coatings. The valve clip includes a push rod, the coatings, and a proximal clamping plate, and a distal clamping plate. The proximal clamping plate and the distal clamping plate extend radially outwardly relative to the push rod. The distal clamping plate is connected to the push rod. The proximal clamping plate is arranged between the push rod and the distal clamping plate. A valve holding space is formed between the proximal clamping plate and the distal clamping plate. The push rod is capable of driving the distal clamping plate to be expanded radially. The proximal clamping plate is capable of expanding toward the distal clamping plate by an elastic strain of the proximal clamping plate and is configured to clamp a valve tissue received in the valve holding space.

Bone anchors and bone anchor insertion systems are provided that enable smaller bone holes for inserting a bone anchor by eliminating the need for a cannula. Smaller bone holes may help reduce patient recovery times. The provided bone anchor includes two flexible wings extending from a base portion that splay away from the base portion's central axis at rest, though may be bent towards or away from the central axis in response to an applied force. The bone anchor includes a drive feature that enables an inserter to couple and decouple to the bone anchor. A surgeon may drive the bone anchor through a bone hole via the coupled inserter while the bone hole maintains the bone anchor in a compressed state, and may decouple the inserter when the bone anchor is properly positioned, thereby eliminating the need for a cannula.

Fixation device for fixation of leaflets of a heart valve includes a central assembly and at least one arm moveably coupled to the central assembly. The at least one arm includes a body portion having a first end and a second end and a longitudinal axis defined therebetween, the second end being moveable between a closed position and an open position, the body portion having opposing body lateral sides, each body lateral side extending between the first end and the second end, the body portion having a body portion width defined between the opposing body lateral sides. The at least one arm further includes first and second nondeformable wing extensions, each wing extension extending laterally from a respective lateral side, each wing extension having a lateral outer edge, wherein a maximum arm width is defined between the outer lateral edge of the first wing extension and the outer lateral edge of the second wing extension. The fixation device further includes at least one gripping element moveable relative to the at least one arm to capture a native leaflet therebetween.

A method is disclosed for removing a vascular occlusion, such as a clot, from a blood vessel. A tubular sheath is inserted into the vessel and a self-expanding Nitinol mesh filter is deployed from a distal end of the tubular sheath at a location proximal to a clot. An inner catheter is advanced through the tubular sheath and through the mesh filter for contacting the clot. An expandable agitation element is provided along a distal end portion of the inner catheter for cutting or chopping the clot, thereby facilitating removal of the clot and improving blood flow through the vessel. Resulting clot particles are captured by the mesh filter. Negative pressure may be applied along a proximal end portion of the sheath for aspirating remaining particles. Certain embodiments of the method are well-suited for treating deep vein thrombosis and do not require the use of thrombolytic drugs.