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Stent Design Articles & Analysis

11 news found

Reflow Medical Completes DEEPER LIMUS Clinical Trial Enrollment

Reflow Medical Completes DEEPER LIMUS Clinical Trial Enrollment

Reflow Medical, Inc., a California-based medical device company, has completed enrollment in the DEEPER LIMUS clinical trial (NCT04162418) to evaluate the Temporary Spur Stent System, a patented device designed to treat long, diffuse and severely calcified infrapopliteal disease. The system allows for uniform expansion of the stent to maximize ...

ByReflow Medical, Inc.


Enrollment Completed In Reflow Medical’s DEEPER OUS Clinical Trial

Enrollment Completed In Reflow Medical’s DEEPER OUS Clinical Trial

Reflow Medical, Inc. announces that it has completed patient enrollment in the DEEPER OUS clinical trial (NCT03807531) for the company’s Temporary Spur Stent System, a novel device that features a retrievable stent designed for complex infrapopliteal disease. 106 patients have now been enrolled in the prospective, nonrandomized trial in ...

ByReflow Medical, Inc.


Vesper Medical Announces Completion of Enrollment in the VIVID Clinical Trial

Vesper Medical Announces Completion of Enrollment in the VIVID Clinical Trial

The Vesper DUO Stent System is designed to be the next generation venous stent technology, uniquely engineered to address the challenges of deep vein obstruction. ...

ByVesper Medical, Inc.


Stacy Enxing Seng Joins the Vesper Medical Board of Directors

Stacy Enxing Seng Joins the Vesper Medical Board of Directors

“The Duo Venous Stent system and the VIVID Trial are clearly designed with the improvement of deep venous disease treatment in mind. ...

ByVesper Medical, Inc.


Advanced Bifurcation Systems Announces First Closing of Series A Financing

Advanced Bifurcation Systems Announces First Closing of Series A Financing

(ABS), a Livermore, CA-based maker of the ABS System, a proprietary stent delivery system that is specifically designed to efficiently treat coronary bifurcation lesions, is pleased to announce the first closing of an $11 million Series A equity financing. ...

ByAdvanced Bifurcation Systems


Vesper Medical Announces First Enrollment in the VIVID Trial

Vesper Medical Announces First Enrollment in the VIVID Trial

The Vesper DUO Stent System is designed to be the next generation venous stent technology, uniquely engineered to address the challenges of deep vein obstruction. ...

ByVesper Medical, Inc.


BioMimics 3D US launch

BioMimics 3D US launch

Veryan Medical (Horsham, UK) today announced that it has launched the innovative BioMimics 3D Vascular Stent System in the US. The BioMimics 3D self-expanding, nitinol stent features a highly-differentiated, helical centre-line design that has achieved excellent clinical outcomes in clinical trials, including a pivotal study with 3-year ...

ByVeryan Medical Ltd.


Cerus Endovascular Receives CE Mark Approval for its Contour 021 device

Cerus Endovascular Receives CE Mark Approval for its Contour 021 device

Cerus Endovascular Ltd., a privately-held, commercial stage medical device company, today announced that it has received CE Mark approval for its state of the art CerusEndo MC 021 microcatheter, designed to allow physicians to access tortuous neurovasculature and deliver therapeutic devices to intended targets. ...

ByCerus Endovascular Inc.


Reflow Medical Enrolls First Patients In The DEEPER LIMUS Study Of The Temporary Spur Stent System

Reflow Medical Enrolls First Patients In The DEEPER LIMUS Study Of The Temporary Spur Stent System

Reflow Medical, Inc., a California-based medical device company, has enrolled the first patients in A Non-Randomized Pilot Study of the Temporary Spur Stent System for the Treatment of Lesions Located in the InfraPoplitEal Arteries Using a LIMUS-base Drug-coated Balloon (DEEPER LIMUS). ...

ByReflow Medical, Inc.


Medinol Completes Enrollment of EluNIR-HBR Study

Medinol Completes Enrollment of EluNIR-HBR Study

EluNIR is Medinol’s sixth generation coronary stent featuring the unique WiZeCell™ stent design which minimizes strut dimensions leading to the lowest possible metal footprint. Combined with a spatially optimized drug delivery, the EluNIR stent is designed to promote rapid vascular healing. In the ...

ByMedinol


FDA Grants NEXUS Aortic Arch Stent Graft System Breakthrough Designation

FDA Grants NEXUS Aortic Arch Stent Graft System Breakthrough Designation

Endospan, a pioneer in off-the-shelf endovascular repair of aortic arch disease was recently granted Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA) for the NEXUS™ Aortic Arch Stent Graft System. ...

ByEndospan Ltd.

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