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Top Endovascular Today News

Medtronic Stock Gains as CMS Proposes Coverage for Renal Denervation
Medicare · United States

Medtronic Stock Gains as CMS Proposes Coverage for Renal Denervation

Coverage: 2 sources
Palo Alto, CA, July 10, 2025 (GLOBE NEWSWIRE) -- Recor Medical, Inc. (“Recor”) and its parent company, Otsuka Medical Devices Co., Ltd. (“Otsuka Medical Devices”), today announced their support for the Centers for Medicare and Medicaid Services’ (CMS) proposed National…See the Story
Cook’s Zenith Iliac Branch Device Approved and Launched in United States - Endovascular Today
United States · United States

Cook’s Zenith Iliac Branch Device Approved and Launched in United States - Endovascular Today

July 14, 2025—Cook Medical announced that its Zenith iliac branch device (ZBIS) is now commercially available in the United States. The first implantations of the device have been performed at several centers across the country. The company advised that on May 30 the ZBIS device received FDA approval as an endovascular treatment option for aortoiliac or iliac aneurysmal disease. According to Cook Medical, ZBIS—when used with the necessary additi…Read Article
Gore Announces Expansion of Mdr Indication for the Gore® Viabahn® Vbx Balloon-Expandable Stent Graft

Gore Announces Expansion of Mdr Indication for the Gore® Viabahn® Vbx Balloon-Expandable Stent Graft

Gore announces expansion of MDR indication for the GORE® VIABAHN® VBX balloon-expandable endoprosthesis as a bridging stentSee the Story

InspireMD’s CGuard Prime Carotid Stent System Launched in United States - Endovascular Today

July 9, 2025—InspireMD, Inc. announced the commercial launch of the CGuard Prime carotid stent system in the United States. On June 24, the company announced FDA premarket approval of the device. According to the company, the CGuard Prime is designed to minimize both early and late embolism risk by trapping potential emboli against the arterial wall while preserving external carotid artery perfusion. InspireMD stated that the device’s features i…Maryland · MarylandRead Article

Verge Medical Acquires RoVo™ System to Advance Peripheral Embolic Protection

100% Center coverage: 1 sources
CAMPBELL, Calif., June 30, 2025 /PRNewswire/ -- Verge Medical, a privately held medical technology company focused on advancing physician-driven solutions to address persistent gaps in vascular care, today announced the acquisition of the RoVo™ System and its patented Temporary Occlusion Embolectomy (TOE) technology from 2MG Medical. The acquisition enhances Verge's expandingUnited States · United StatesSee the Story

RESCUE-II Study Published On Thrombolex Bashir Catheter for PE - Endovascular Today

June 25, 2025—Thrombolex, Inc., a developer of treatments for arterial and venous thromboembolic diseases, announced the publication of the results from the RESCUE-II study. The study assessed the company’s Bashir endovascular catheter (BEC) in treating pulmonary embolism (PE) on the table (OTT). The study was published by Vladimir Lakhter, DO, et al in JACC: Advances. “The RESCUE-II study demonstrated encouraging safety and feasibility, while r…Read Article

Embolization Has Received FDA 510(k) Clearance for Its NED Embolization Device - Interventional News

Embolization has announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA). The Nitinol Enhanced Device (NED) is a vascular embolization device intended for arterial and venous embolization in peripheral vasculature.  Vascular embolization is a minimally invasive procedure where a physician intentionally blocks a blood vessel using tiny materials such as coils, particles or glue. This stops bleeding, reduces …United States · United StatesSee the Story

First Patient Enrolled in RECOVER-AV Trial of AlphaVac F18 System for Treatment of Acute PE - Cardiovascular News

AngioDynamics has announced the first patient has been enrolled in the RECOVER-AV clinical trial, a prospective, multicentre, international, single-arm study evaluating the AlphaVac multipurpose mechanical aspiration (MMA) F1885 system in the treatment of acute, intermediate-risk pulmonary embolism (PE). The study follows the US Food and Drug Administration (FDA) 510(k) clearance of the AlphaVac F1885 system for the treatment of PE in the USA in…Canada · CanadaSee the Story

Anaconda ANA5 Funnel Catheter for Ischemic Stroke Approved in Europe - Endovascular Today

June 18, 2025—Anaconda Biomed, SL, announced that it has received CE Mark certification for its ANA5 advanced neurovascular access funnel catheter. The CE Mark enables eventual commercial availability of the device across the European Union, noted Anaconda, a developer of neurothrombectomy devices based in Barcelona, Spain. Anaconda noted that the ANA5 funnel catheter features a vessel-matching diameter funnel to maximize clot capture in mechani…Maryland · MarylandRead Article

Inquis’ Aventus Thrombectomy System Cleared to Treat PE - Cardiac Interventions Today

June 16, 2025—Inquis Medical announced that its Aventus mechanical thrombectomy system has received FDA 510(k) clearance for an expanded indication to treat pulmonary embolism (PE). The device was previously cleared by the FDA for use in the peripheral vasculature. According to Inquis, the Aventus system incorporates the company’s tissue-sensing technology to help physicians distinguish the type of tissue in contact with the catheter tip in real…Maryland · MarylandSee the Story

InspireMD's Embolic Prevention System Gains CE Mark Approval

InspireMD’s CGuard Prime Embolic Prevention System (EPS) has secured CE Mark approval under the European MDR for stroke prevention.The post InspireMD’s embolic prevention system gains CE Mark approval appeared first on Medical Device Network.United States · United StatesSee the Story

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