Abstract: The present disclosure relates to medical devices including occlusion devices, clot retrieval systems, and stents. More particularly, the medical devices described herein measure characteristics for intravascular treatment sites. The medical devices may include pressure sensors and/or length sensors that may be used to determine the effectiveness of the medical devices during or after treatment. These sensors may be particularly helpful when used on an occlusion device or a clot removal device.

Abstract: Described herein are durable coatings, i.e. for medical devices, and methods of forming the coatings.

Abstract: Described herein are durable coatings, i.e. for medical devices, and methods of forming the coatings.

Abstract: A clot retrieval device is disclosed. In some embodiments, the device utilizes augmented radiopacity to improve imaging, an internal tensioning member, a plurality of connected components useful to engage larger clots, and/or a distal end configuration designed to enhance clot retention.

Abstract: A clot retrieval device is disclosed. In some embodiments, the device utilizes augmented radiopacity to improve imaging, an internal tensioning member, a plurality of connected components useful to engage larger clots, and/or a distal end configuration designed to enhance clot retention.

Abstract: This specification is directed to stents that are configured to better deploy and remain implanted across a fusiform aneurysm. Specifically, these stents include one or more anchoring members that radially expand within a fusiform aneurysm. In some instances, the anchoring members radially expand to a diameter that is larger than that of regions of vessels adjacent to the fusiform aneurysm to help prevent stent migration. The anchoring members can be a bulbous layer, a plurality of loops, a plurality of arms, a plurality of longitudinal wires, or one or more hydrogel rings.

Abstract: The present disclosure relates to medical devices including occlusion devices, clot retrieval systems, and stents. More particularly, the medical devices described herein measure characteristics for intravascular treatment sites. The medical devices may include pressure sensors and/or length sensors that may be used to determine the effectiveness of the medical devices during or after treatment. These sensors may be particularly helpful when used on an occlusion device or a clot removal device.

Abstract: A distal aspiration catheter comprises catheter body having a central lumen and at least one luminal channel. An aspiration source is configured to attach to a proximal end/luer hub of the central lumen. Each luminal channel includes one mandrel and a distal portion of the mandrel extends into a distal portion in the central lumen. When the aspiration source is activated, a clot/emboli lodged in a blood vessel is partially ingested into the distal portion of the central lumen. The distal portion of the mandrel can move into the partially ingested clot to induce clot fatigue. The fatigued clot can be removed completely by a single pass of the distal aspiration catheter.

Abstract: Described herein are durable coatings, i.e. for medical devices, and methods of forming the coatings.

Abstract: The present disclosure relates to a delivery catheter and the stepwise release of a stent from the catheter into the vasculature of a patient, as well as a loading device for a transcatheter heart valve (THV) prosthesis.

Abstract: The present disclosure relates to a delivery catheter and the stepwise release of a stent from the catheter into the vasculature of a patient, as well as a loading device for a transcatheter heart valve (THV) prosthesis.

Abstract: A transcatheter valve prosthesis includes an expandable tubular stent, a prosthetic valve within the stent, and an anti-paravalvular leakage component coupled to and encircling the tubular stent. The anti-paravalvular leakage component includes a radially-compressible annular scaffold, which is a sinusoidal patterned ring of self-expanding material, and an impermeable membrane extending over the annular scaffold. The anti-paravalvular leakage component has an expanded configuration in which at least segments of the annular scaffold curve radially away from the tubular stent. Alternatively, the anti-paravalvular leakage component includes a plurality of self-expanding segments and an annular sealing element coupled to inner surfaces of the segments. The anti-paravalvular leakage component has an expanded configuration in which the segments curve radially away from the tubular stent and the annular sealing element is positioned between an outer surface of the tubular stent and inner surfaces of the segments.

Abstract: A clot retrieval device is disclosed. In some embodiments, the device utilizes augmented radiopacity to improve imaging, an internal tensioning member, a plurality of connected components useful to engage larger clots, and/or a distal end configuration designed to enhance clot retention.

Abstract: A vascular prosthesis utilizing drawn-filled tubing (DFT) wire to aid in visualizing the prosthesis without needing supplemental radiopaque material is described.

Abstract: Described herein is a braided stent having have a plurality of different segments that can reduce or eliminate foreshortening and allow the proximal end of the stent to more reliably open when deployed in a curved vessel. The segments can be connected together by interlocking loops positioned at the end of each segment and can be formed of one or more radially progressing wave patterns.

Abstract: A transcatheter valve prosthesis includes an expandable tubular stent, a prosthetic valve within the stent, and an anti-paravalvular leakage component coupled to and encircling the tubular stent. The anti-paravalvular leakage component includes a radially-compressible annular scaffold, which is a sinusoidal patterned ring of self-expanding material, and an impermeable membrane extending over the annular scaffold. The anti-paravalvular leakage component has an expanded configuration in which at least segments of the annular scaffold curve radially away from the tubular stent. Alternatively, the anti-paravalvular leakage component includes a plurality of self-expanding segments and an annular sealing element coupled to inner surfaces of the segments. The anti-paravalvular leakage component has an expanded configuration in which the segments curve radially away from the tubular stent and the annular sealing element is positioned between an outer surface of the tubular stent and inner surfaces of the segments.

Abstract: A device for crimping an expandable medical device and loading the expandable medical device into a delivery system includes an actuator, a compression assembly, and a pusher. The compression assembly is disposed in a compression chamber of the actuator and includes a plurality of compression elements coupled to each other to form a central cavity. The compression elements are coupled to the actuator such that rotation of the actuator causes the compression elements to rotate such that the central cavity radially compresses from an expanded configuration to a compressed configuration. The pusher includes a pusher rod and is configured to translate relative to the actuator towards the compression chamber when the cavity is in the compressed configuration such that the pusher rod may enter the cavity and push the medical device out of the cavity into delivery system.

Abstract: A device for crimping an collapsible device and loading the collapsible device into a delivery system, includes a crimping tool configured to radially crimp at least a portion of the collapsible device, a loading tool configured to load at least a portion of the collapsible device into a delivery system, and a housing that houses at least one of the crimping tool and loading tool, wherein the device is configured to crimp and load the collapsible device without requiring manual repositioning of the collapsible device. Methods of crimping an collapsible device and loading the collapsible device into a delivery system are also disclosed.

Abstract: A device for crimping an expandable medical device and loading the expandable medical device into a delivery system includes an actuator, a compression assembly, and a pusher. The compression assembly is disposed in a compression chamber of the actuator and includes a plurality of compression elements coupled to each other to form a central cavity. The compression elements are coupled to the actuator such that rotation of the actuator causes the compression elements to rotate such that the central cavity radially compresses from an expanded configuration to a compressed configuration. The pusher includes a pusher rod and is configured to translate relative to the actuator towards the compression chamber when the cavity is in the compressed configuration such that the pusher rod may enter the cavity and push the medical device out of the cavity into delivery system.

Abstract: A transcatheter valve prosthesis includes an expandable tubular stent, a prosthetic valve within the stent, and an anti-paravalvular leakage component coupled to and encircling the tubular stent. The anti-paravalvular leakage component includes a radially-compressible annular scaffold, which is a sinusoidal patterned ring of self-expanding material, and an impermeable membrane extending over the annular scaffold. The anti-paravalvular leakage component has an expanded configuration in which at least segments of the annular scaffold curve radially away from the tubular stent. Alternatively, the anti-paravalvular leakage component includes a plurality of self-expanding segments and an annular sealing element coupled to inner surfaces of the segments. The anti-paravalvular leakage component has an expanded configuration in which the segments curve radially away from the tubular stent and the annular sealing element is positioned between an outer surface of the tubular stent and inner surfaces of the segments.