A medical securing device for securing an object with a securing member into a tissue comprises an elongated sheath with proximal and distal ends, and a securing member introduction device having proximal and distal ends. The securing member comprises first and second ends. The distal end of the securing member introduction device is configured to extend the second end of the securing member from the sheath and introduce it to or through the tissue via an introduction movement so to secure the portion of the securing member to the object and/or to the tissue. This is advantageously configured to happen without extending the securing member introduction device through the tissue whereupon no extra hole is made to the tissue by the securing member introduction device.

An apparatus can include a first flexible member having first and second ends and a first body extending therebetween, where the first body defines a first passage portion. A second flexible member can have first and second ends and a second body extending therebetween, where the second body defines second and third passage portions. The first end of the first flexible member passes into and through the second passage portion such that the first end extends outside of the second passage portion, and the second end of the first flexible member passes into and through the third passage portion such that the second end extends outside of the third passage portion. The first and second ends of the second flexible member pass into and through the first passage portion to form a self-locking adjustable flexible member construct.

Devices and methods for treating or repairing a heart are disclosed. The device includes at least one radially expandable tissue-engaging element, an elongate member (e.g., suture) coupled to the expandable element, and a locking mechanism (e.g., locking clip, suture knot). The expandable element may be anchored to heart tissue within the heart, such as in the left ventricle, with the elongate member extending from the expandable element and across a heart chamber to a second location such as the heart apex where the elongate member is held by the locking mechanism.

A barbed suture including a body with barbs on the periphery, a pointed end, and an anchor at one end to resist movement of the suture in the direction of the pointed end is provided. One or more limbs on the anchor may be provided, which may be arcuate, of varying lengths, and of varying distribution about the periphery of the suture body. Other anchor designs are provided. Methods of placing single-directional and bi-directional barbed sutures to approximate the tissue on each side of a wound and to position and support tissue in the absence of a wound, as in cosmetic surgery, are provided, and may include terminal J-stitches or S-stitches. Methods of placement may be made with sharp, pointed ends, which may be needles, or insertion devices. Sinusoidal patterns of sutures that have amplitudes generally perpendicular to the resultant holding force of the suture are provided.

Barbed surgical sutures are prepared with a bioactive agent thereon. In embodiments, the bioactive agent may be an antimicrobial or clotting agent deposited within the angle formed by the barb and the suture body. Placement of the bioactive agent in the angle between the barb and suture body enhances the delivery of the bioactive agent to wound tissue at the point of contact.

An embodiment includes a chordal replacement system comprising: a pledget coupled to a first suture length and at least one of a first needle and a first ferrule; a second suture length coupled to the pledget and at least a second needle; and a third suture length coupled to the pledget and at least a third needle; wherein the second and third suture lengths are not monolithic with each other and do not constitute a single suture. Other embodiments are described herein.

A wound closure device can be provided as described herein. In an example, the wound closure device includes a first suture segment having a first suture configuration and a second suture segment having a second suture configuration. The first and second suture configurations can be different from each other. For example, the first suture configuration can includes a first set of characteristics such as barbed or non-barbed, barb sizes, filament sizes, colors, materials, and/or the like and the second suture configuration can include a second set of characteristics such as barbed or non-barbed, barb sizes, filament sizes, colors, materials and/or the like that can be different from the first set of characteristics. The wound closure device can further include connecting section configured to provide a transition from the first suture segment to the second suture segment.

An exemplary tissue compression device for forming an anastomosis includes a first device portion having a first mating surface, a first base wall recessed from the first mating surface so as to define a first inner recess, and a first set of suture bores extending through the first base wall and opening to an outer periphery of the first device portion. A second device portion of the device has a second mating surface, a second base wall recessed from the second mating surface so as to define a second inner recess, and a second set of suture bores extending through the second base wall and opening to an outer periphery of the second device portion. The first and second device portions are configured to compress tissue positioned between the first and second mating surfaces.

The present disclosure is directed towards an apparatus for holding a suture. The apparatus may comprise a carrier including a base. The carrier may be configured to retain a cover over the base. The base may be configured to mount the carrier on a fixture and include a primary wrapping path disposed thereon, the wrapping path for wrapping at least a portion of a suture thread. The apparatus may include a plurality of suture retaining canopies located at an outer portion of the primary wrapping path and projecting from the base. The suture retaining canopies may be configured to facilitate retaining a suture thread within the primary suture path. The apparatus may also include a needle retainer disposed on the base. The needle retainer may include at least one slot configured to retain a needle.

The present disclosure relates to a device for assisting in communicably coupling a first organ body with a second organ body by employing a plurality of arc-shaped tissue connector devices comprising a tissue connector body with a proximal and distal end, and a method for manufacturing such a device. The device comprises a curved frame having a principle axis and configured to embrace, at least partially, the first organ body, the curved frame configured to receive a plurality of tissue connector devices which extend from a proximal end thereof coupled to the curved frame and terminate in a free distal end. The disclosure further relates to a tissue connector device, a holder for tissue connector devices and a tissue-collar manipulating device, and a method of coupling a first and a second organ body using such device.