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Top Endovascular Today News

Verge Medical Acquires RoVo™ System to Advance Peripheral Embolic Protection
United States · United States

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 expandingSee the Story
First Patient Enrolled in RECOVER-AV Trial of AlphaVac F18 System for Treatment of Acute PE - Cardiovascular News
Canada · Canada

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…See the Story
Embolization Has Received FDA 510(k) Clearance for Its NED Embolization Device - Interventional News
United States · United States

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 …See 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

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

Medtronic plc (NYSE:MDT) Shares Bought by Verity & Verity LLC

100% Center coverage: 1 sources
Verity & Verity LLC increased its stake in Medtronic plc (NYSE:MDT - Free Report) by 9.7% during the first quarter, according to its most recent filing with the Securities & Exchange Commission. The fund owned 196,199 shares of the medical technology company's stock after acquiring an additionaDublin, Ireland · DublinSee the Story

FDA Clears CT-Based AI Software for Subdural Collections

The AI-powered Viz Subdural Plus reportedly provides automated measurements and labeling of subdural collections, including subdural hemorrhages (SDHs), based on non-contrast CT scans.FDA · United StatesSee the Story

Medtronic’s GSR-DEFINE Study of Symplicity Spyral RDN System Enrolls First United States Patient - Cardiac Interventions Today

June 11, 2025—Medtronic announced the treatment of the first patient in the United States in the Global SYMPLICITY Registry (GSR) DEFINE. The clinical study is documenting the safety and effectiveness of the company’s Symplicity Spyral renal denervation (RDN) system in a real-world setting. The company stated that the first United States procedure was performed by Stan Thornton, MD, of Thomas Hospital, an affiliate of Infirmary Health in Fairhop…Maryland · MarylandSee the Story

Machine Learning to Predict Penumbra Core Mismatch in Acute Ischemic Stroke Using Clinical Note Data

100% Center coverage: 1 sources
In acute ischemic stroke due to large-vessel occlusion (AIS-LVO), late-window endovascular thrombectomy (EVT) decisions depend on penumbra-to-core (P:C) mismatch from computed tomographic perfusion (CTP). We developed multiple machine learning (ML) models to predict P:C ratios from a retrospectively-identified cohort of AIS-LVO patients who underwent CTP within 30 min of initial neuroimaging, using non-imaging electronic health record (EHR) data…FDA · CaliforniaSee the Story

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