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Top Interventional News News

Medtronic Recall After 33 Injuries; Private Equity in Gastroenterology; MASLD Crisis
Health · United States

Medtronic Recall After 33 Injuries; Private Equity in Gastroenterology; MASLD Crisis

100% Center coverage: 3 sources
(MedPage Today) -- The FDA announced a recall of certain Medtronic Bravo esophageal pH monitoring capsules, which help in diagnosing gastroesophageal reflux, following 33 reports of serious injuries. Despite no-cost provisions in the Affordable...See the Story
Onco-Innovations Enters Agreement with Nucro-Technics for IND-Enabling Studies, Taking a Key Step Toward Human Trials
Amsterdam, Netherlands · Amsterdam

Onco-Innovations Enters Agreement with Nucro-Technics for IND-Enabling Studies, Taking a Key Step Toward Human Trials

Coverage: 2 sources
VANCOUVER, BC / ACCESS Newswire / July 4, 2025 / Onco-Innovations Limited (CBOE CA:ONCO)(OTCQB:ONNVF)(Frankfurt:W1H,WKN: A3EKSZ) ("Onco" or the "Company") is pleased to announce that it has entered into an agreement with Nucro-Technics Inc. ("Nucro-Technics"), dated July 3, 2025, pursuant to…See the Story
E2 concludes enrolment of pulmonary embolism thrombectomy system trial

E2 concludes enrolment of pulmonary embolism thrombectomy system trial

100% Center coverage: 1 sources
E2 has completed enrolment of subjects in the pivotal cohort of its ENGULF trial, involving the Hēlo PE Thrombectomy System.The post E2 concludes enrolment of pulmonary embolism thrombectomy system trial appeared first on Medical Device Network.See 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

Vivasure Submits PMA For Vascular Closure System To FDA - Data Intelligence

The system is a fully absorbable, sutureless closure device for use after percutaneous cardiovascular procedures. Credit: Max Acronym / Shutterstock. Irish company Vivasure Medical has submitted an application seeking premarket approval (PMA) from the US Food and Drug Administration (FDA) for its PerQseal Elite vascular closure system intended for arterial procedures. This submission is supported by the outcomes of the PATCH study and the system…FDA · United StatesSee the Story

StentIt launches first-in-human trial of bioresorbable stent to treat below-the-knee CLTI - Interventional News

StentIt has announced the successful implantation of its Resorbable Fibrillated Scaffold (RFS). As part of the VITAL-IT 1 study, patients with chronic limb-threatening ischaemia (CLTI) below the knee have successfully been treated using the RFS implant. In this clinical procedure, revascularisation was achieved using an endovascular approach to restore blood flow to the foot. StentIt’s RFS device is a bioresorbable stent built from microfibers, …Graz · GrazRead 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

Gore Tag thoracic branch endoprosthesis receives expanded FDA approval for endovascular aortic arch repair - Interventional News

Gore Tag Gore has announced that the Gore Tag thoracic branch endoprosthesis (TBE) is now approved by the US Food and Drug Administration (FDA) for use in Zones 0 and 1, expanding its indication for the endovascular repair of lesions in the aortic arch and descending thoracic aorta while preserving flow to a single aortic arch branch vessel. The device becomes the first off-the-shelf, single-branch thoracic endoprosthesis indicated across Zones …United States · United StatesRead Article

UK Regulator Overhauls Medical Device Regulation

100% Center coverage: 1 sources
Major changes to medical device regulations in the UK have come into force with an overhaul of post-market surveillance requirements.Regulation · United KingdomSee the Story

Penumbra's Revolutionary PE Treatment Trial Hits 100-Patient Mark, Results Could Transform Blood Clot Care

First-of-its-kind RCT evaluates computer-assisted thrombectomy vs. standard care in 100 PE patients. Trial completed ahead of schedule. See potential impact.See the Story

Future-focused IR imaging for a broad procedure mix - Interventional News

This supplement is sponsored by Siemens Healthineers AG. In this supplement: David Madoff (Yale School of Medicine, New Haven, USA) highlights how syngo DynaCT and Embolization Guidance on the ARTIS icono system enhance tumour targeting in liver embolization. Maximilian de Bucourt (Charité–Universitätsmedizin, Berlin, Germany) showcases how myNeedle Guide with integrated laser cross supports a wide range of percutaneous procedures by enabling p…Mount Sinai, New York · Mount SinaiRead Article

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