A61F2/954

Branched graft assembly method in vivo

A branched graft method includes securing a first end of a branch graft into a first conduit and subsequently moving the second end into a second conduit. The first conduit may be a branch vessel, such as a renal artery and the second conduit may be a main graft that extends over an aortic aneurysm. The branch graft may be deployed starting at an offset distance from the first end, thereby preventing the deployed portion from insertion into the first conduit and predetermining the insertion length into the target vessel. The first end may then be deployed to secure the first end to the first conduit. A branch graft may be a self-expanding stent graft having one or more ripcords, and/or a serpentine ripcord that enables non-linear deployment of the branch graft, or deployment that does not progress from one end to the opposing end.

Modular stent graft systems and methods with inflatable fill structures
11497597 · 2022-11-15 · ·

An apparatus includes a first stent graft that is at least partially insertable into a first blood vessel. The first stent graft has a first end, a second end, an inside surface, and an outside surface. The apparatus also includes an inflatable fill structure fixed to a portion of the outside surface of the first stent graft. The inflatable fill structure includes an outer membrane that is configured to extend beyond the first end of the first stent graft when the inflatable fill structure is in a filled state.

Modular stent graft systems and methods with inflatable fill structures
11497597 · 2022-11-15 · ·

An apparatus includes a first stent graft that is at least partially insertable into a first blood vessel. The first stent graft has a first end, a second end, an inside surface, and an outside surface. The apparatus also includes an inflatable fill structure fixed to a portion of the outside surface of the first stent graft. The inflatable fill structure includes an outer membrane that is configured to extend beyond the first end of the first stent graft when the inflatable fill structure is in a filled state.

Endoluminal Stent and Endoluminal Stent System

The present invention relates to an endoluminal stent and an endoluminal stent system, with the endoluminal stent being delivered to a site at which it is to be implanted by means of a delivery device comprising a sheath for receiving the endoluminal stent. The endoluminal stent comprises a hollow tube body portion, a connection portion and a flange portion, wherein the tube body portion is connected to one end of the connection portion, the flange portion has a connection end and a suspended end opposite one another, with the connection end being connected to the other end of the connection portion in a turning connection, and the suspended end being suspended, the flange portion comprising a flange section bare wave ring made of an elastic material; the suspended end is located at a distal side of the connection end when the endoluminal stent is in a natural state; the suspended end is located at a proximal side of the connection end when the endoluminal stent is received in the sheath; and after the flange portion is released from the sheath, the flange portion automatically turns over, and the suspended end moves from the proximal side of the connection end to the distal side of the connection end. The endoluminal stent of the present invention can enhance the anchoring force thereof.

Endoluminal Stent and Endoluminal Stent System

The present invention relates to an endoluminal stent and an endoluminal stent system, with the endoluminal stent being delivered to a site at which it is to be implanted by means of a delivery device comprising a sheath for receiving the endoluminal stent. The endoluminal stent comprises a hollow tube body portion, a connection portion and a flange portion, wherein the tube body portion is connected to one end of the connection portion, the flange portion has a connection end and a suspended end opposite one another, with the connection end being connected to the other end of the connection portion in a turning connection, and the suspended end being suspended, the flange portion comprising a flange section bare wave ring made of an elastic material; the suspended end is located at a distal side of the connection end when the endoluminal stent is in a natural state; the suspended end is located at a proximal side of the connection end when the endoluminal stent is received in the sheath; and after the flange portion is released from the sheath, the flange portion automatically turns over, and the suspended end moves from the proximal side of the connection end to the distal side of the connection end. The endoluminal stent of the present invention can enhance the anchoring force thereof.

STENT SYSTEM FOR TREATING DIFFUSED LESIONS IN BIFURCATED ARTERIES

A stent system is disclosed. The stent system includes a balloon catheter having a balloon with a proximal zone, a transition zone and a distal zone including progressively decreasing diameters respectively. The stent of a pre-defined length includes a main branch segment, a transition segment and a side branch segment. The stent includes an expanded state and a crimped state. The stent is mounted over the balloon in the crimped state such that the main branch segment is mounted over the proximal zone, the transition segment is mounted over the transition zone and the side branch segment is mounted over the distal zone. In expanded state, the main branch segment, the transition segment and the side branch segment of the stent correspond to the respective zones of the balloon. The transition segment includes plural rows of elongated members connected to each other.

STENT SYSTEM FOR TREATING DIFFUSED LESIONS IN BIFURCATED ARTERIES

A stent system is disclosed. The stent system includes a balloon catheter having a balloon with a proximal zone, a transition zone and a distal zone including progressively decreasing diameters respectively. The stent of a pre-defined length includes a main branch segment, a transition segment and a side branch segment. The stent includes an expanded state and a crimped state. The stent is mounted over the balloon in the crimped state such that the main branch segment is mounted over the proximal zone, the transition segment is mounted over the transition zone and the side branch segment is mounted over the distal zone. In expanded state, the main branch segment, the transition segment and the side branch segment of the stent correspond to the respective zones of the balloon. The transition segment includes plural rows of elongated members connected to each other.

STENT RETENTION
20230042061 · 2023-02-09 ·

A system and method for a stent delivery system, the delivery system having a catheter and a balloon coupled to a distal portion of the catheter. The catheter with the radially expandable member is inserted into a cavity in a mold. Heat and pressure are applied for a period of time which inflates the balloon and imparts a shape memory to a portion of the balloon. The balloon is removed from the cavity of the mold with a shape memory.

METHODS AND SYSTEMS FOR ESTABLISHING RETROGRADE CAROTID ARTERIAL BLOOD FLOW

Interventional procedures on the carotid arteries are performed through a transcervical access while retrograde blood flow is established from the internal carotid artery to a venous or external location. A system for use in accessing and treating a carotid artery includes an arterial access device, a shunt fluidly connected to the arterial access device, and a flow control assembly coupled to the shunt and adapted to regulate blood flow through the shunt between at least a first blood flow state and at least a second blood flow state. The flow control assembly includes one or more components that interact with the blood flow through the shunt.

SYSTEMS, DEVICES, AND METHODS FOR COUPLING A PROSTHETIC IMPLANT TO A FENESTRATED BODY
20230032657 · 2023-02-02 ·

Devices, systems, and methods for implanting a patient-specific prosthesis at a treatment site in a patient are disclosed herein. In some embodiments, a patient-specific prosthesis includes a tubular graft and a coupling member. A fenestration can be disposed in the tubular graft, the fenestration corresponding to a predicted branch blood vessel location. The coupling member can be disposed about the fenestration. The coupling member can include a coil configured to expand from a first configuration to a second configuration in response to the application of an expanding force. The coil can be configured to contract to a third configuration upon removal of the expanding force.