Abstract: Surgical forceps for removing varicose veins with surgical forceps and related methods are provided. The surgical forceps comprise an elongate tubular sheath, two jaws mounted movably relative to each other around a pivot axis at a distal end of the tubular sheath, two maneuvering branches each having a ring for the insertion of a finger, and a linkage for transmitting the movement of the maneuvering branches to the jaws. The method comprises inserting a finger in each ring, introducing the surgical forceps into a patient's skin, and moving the maneuvering branches towards one another to move the jaws to a gripping position to grip the varicose veins.

Abstract: This disclosure describes compliant graspers for use in endoscopic surgeries.

Abstract: A system for implanting a repair device onto a native valve of a natural heart to repairing the native valve of a patient during a non-open-heart procedure. The system includes a surgical delivery instrument, a valve repair device, and a gripper control mechanism. The surgical delivery instrument has at least one lumen. The valve repair device is configured to be delivered through the lumen of the surgical delivery instrument and to be attached to a native valve of a patient. The valve repair device includes a pair of paddles, and at least four gripping members. The paddles are movable between an open position and a closed position, and the paddles and the at least four gripping members are configured to attach to the native valve of a patient. The gripper control mechanism is configured to independently move each of the at least four gripping members.

Abstract: A robotic catheter procedure system for performing a procedure to treat a vascular lesion including a bedside system and a remote workstation is provided. The bedside system includes a first percutaneous device including an end section, the end section structured to allow the first percutaneous device to create a bore through the vascular lesion. The bedside system includes a second percutaneous device. The bedside system also includes a first actuating mechanism configured to engage and to impart movement to the first percutaneous device and a second actuating mechanism configured to engage and to impart movement to the second percutaneous device. The remote workstation includes a user interface and a control system operatively coupled to the user interface and to the bedside system.

Abstract: Apparatus for securing an object to bone, the apparatus comprising: an anchor, the anchor comprising: a body comprising an opening for receiving a filament therein; and a locking element movably mounted to the body for selectively locking the filament to the body; and an inserter for deploying the anchor in bone, the inserter comprising: a handle; an overtube extending distally from the handle; a carriage movably mounted to the handle; a shaft movably mounted within the overtube and connected to the carriage and releasably connected to the body of the anchor, the shaft being hollow; and a rod movably mounted within the shaft and connected to the locking element.

Abstract: In a device for stretching the skin, particularly for closing a wound, anchoring elements are anchored in the skin. The anchoring elements are movable on a guide device. First anchoring elements are anchored in the skin of the edge of the wound. Second anchoring elements are adjustable on the guide device in the stretching direction behind the first anchoring elements in relation to and independently of said first anchoring elements.

Abstract: Systems and methods disclosed stimulate nerve growth by applying a tensile (axial pulling) load on a proximal stump of the nerve. This load may be imposed once, at the time of repair. This implementation may be advantageously employed to remove tension away from the repair site, for any number of soft tissues, e.g., nerves, ligaments, tendons, and so on. Alternately, for a larger gap, by progressively elongating a nerve through tensile stimulation, the nerve may regenerate and be fully functional, particularly if elongated at a proper rate. After sufficient regrowth, nerve ends may be reattached, resulting in more complete functional recovery. Two implementations, which have been embodied in prototype devices, also include particularly useful features, one of which uses a screw and clamp with slotted insert design, and the other of which enables the use of sutures or straps to secure the tissue to the clamp.

Abstract: Described herein are apparatus, compositions, systems and associated methods to occlude structures and malformations of the vasculature with radiopaque hydrogel filaments with delayed controlled rates of expansion. Further described is a device for implantation in an animal comprising a difunctional, low molecular weight ethylenically unsaturated shapeable macromer; an ethylenically unsaturated monomer; and a radiopaque element, wherein said device contains no support members. Methods of forming such devices are also disclosed.

Abstract: Apparatus and method for delivering and deploying an intravascular device into the vessel including an outer and inner tube that are axially linked by a housing structure at the proximal end of the catheter, and a retractable sleeve structure having a middle tube and sleeve tip. The sleeve tip is sealed to the inner tube at the distal end, and continuously extends into the middle tube. At the proximal end of the sleeve structure, the middle tube is sealed to either a housing structure or slideable proximal ring, forming a sealed chamber between the inner tube and the sleeve structure. A radial space is formed between the sleeve tip and the inner tube optimized for intravascular device placement. During retraction of the sleeve structure, the fold of the sleeve tip peels away from the device, which expands to its deployed state while minimizing axial forces and friction.

Abstract: Intraocular lens (IOL) insertion apparatus and methods of use are provided and described herein. An example IOL insertion apparatus may include a handpiece body having a distal tip, a deployment chamber having an opening at a distal end of the handpiece body, and a deployment system disposed within the handpiece body. The deployment system can include a deployment carriage movable between proximal and distal positions within the handpiece body and a deployment plunger with a proximal end secured to the deployment carriage and a distal end to engage a folded IOL. The insertion apparatus may further include a damping feature protruding from a wall of the deployment chamber or a portion of the deployment system. The first damping feature may be positioned and arranged to increase a resistance to movement of the deployment system along a portion of a path traveled thereby between the proximal and distal positions.

Abstract: A flexible-manipulator guide member is provided in an inserted portion of a flexible manipulator including the elongated flexible inserted portion, the movable portion disposed at the distal end of the inserted portion, a drive portion disposed at the base end of the inserted portion, and the elongated driving-force transmitting member that transmits motive power of the drive portion to the movable portion, and is provided with a lumen through which the driving-force transmitting member passes in the longitudinal direction, wherein the lumen has a twisted shape about the longitudinal axis of the inserted portion.

Abstract: A connector for fluidly coupling proximal and distal tubular segments of a fluid conduit is provided. In one embodiment, the connector can include a connector body having an outer surface defining a first outer perimeter and an inner surface defining a lumen. The connector can also include a connecting device having an open configuration and a plurality of closed configurations. The connecting device can include first and second members configured to engage each other to secure the fluid conduit to the connector. The connecting device can also include a plurality of closed configurations for securing fluid conduits of different sizes.

Abstract: A tissue bag for surrounding tissue (2) during a surgical procedure comprises a bag body (6) capable of forming an enclosure, an opening (9) in the bag body, and one or more inflatable ribs (8) located on the bag body. The ribs (8) are such that inflation of the one or more ribs to a first extent causes the bag to deploy to an open position in which the bag is capable of being placed over tissue with the tissue received through the opening. Inflation of the one or more ribs (8) to a second further extent causes the bag to envelop the tissue with the opening (9) being smaller in diameter than in the open position. The ribs may each include at least first and second discrete longitudinal portions (10), (11) with an angled end face (15) therebetween.

Abstract: In a device for stretching the skin, particularly for closing a wound, anchoring elements are anchored in the skin. The anchoring elements are movable on a guide device. First anchoring elements are anchored in the skin of the edge of the wound. Second anchoring elements are adjustable on the guide device in the stretching direction behind the first anchoring elements in relation to and independently of said first anchoring elements.

Abstract: The invention pertains to an apparatus comprising a needle configured to define a path through tissue of a patient, tubing configured to slidably receive the needle via a proximal opening, an anchor configured to slidably receive at least a portion of the tubing, and an anchor deployment member comprising a body and an anchor engagement member. Such an apparatus may be used to introduce and anchor an implantable medical device element within a patient.

Abstract: A delivery device for a collapsible prosthetic heart valve includes a support shaft around which a compartment is defined, an inner shaft extending through the support shaft and adapted to slide relative to the support shaft along a longitudinal axis thereof, the inner shaft having a lumen therethrough, and a distal sheath operatively connected at a distal end to the inner shaft and slidable therewith. The compartment may receive the valve in an assembled condition, and may be selectively covered and uncovered by the distal sheath. A first flow path may provide flow communication between the lumen of the inner shaft and the compartment.

Abstract: A suture assembly, including a button having two apertures and a suture defining a lumen and forming a double loop, formed by a double trap having a first end and a second end, opposed to the button. A first portion of the suture is threaded through the trap from the first end to the second end, and a second portion of the suture is threaded through the trap from the second end to the first end. The assembly further defines a first single trap, in which the first portion of the suture is threaded through the lumen between the second end and the button. Also defined by the assembly is a third trap, in which the second portion of the suture is threaded through the lumen between the first end and the button. Finally, the double loop is threaded through the two apertures of the button.

Abstract: The needle holder includes a primary hollow shaft, a secondary hollow shaft attached to the primary hollow shaft in a generally “T” configuration, a pair of extendible jaws rotatably positioned at a distal end of the primary shaft, a trigger mechanism mounted on the primary shaft for selectively extending the jaws, a first rotation member in the primary shaft, a second rotation member in the secondary shaft, a driven gear attached to the first rotation member, and a drive gear attached to the second rotation member and configured to selectively engage the first gear. The jaws are selectively extendible and rotatable.

Abstract: In various examples, a suture anchor includes a sheath including a lumen. A frame member is disposed at least partially within the sheath. The frame member includes at least two suture loops extending from the sheath. The suture loops are configured to receive a suture, wherein tightening of the suture causes compression of the frame member to constrict the lumen of the sheath.

Abstract: The prosthetic joint has at least two members having each a cooperating articulating surface layer on a substrate material. At least one of said articulating surface layers comprises amorphous diamond-like carbon; or Titanium Nitrate (TiN) on a bonding layer bonded to the substrate material. The prosthetic joint provides a reduction of the number of wear debris and shows enhanced dry run properties.