News from Interventional NewsFollowNews from Interventional NewsSee all of Interventional News news coverage in one place. Discover how Interventional News’s media bias informs their coverage and compare with thousands of other news outlets.We’ve discovered 84 headlines written by Interventional News during the past 3 months. The Ground News media bias check for Interventional News is . Scores are assigned by aggregating bias scores from Ad Fontes Media, Media Bias/Fact Check, and All Sides. Interventional News’s factuality rating is Unknown. Ground News calculates this rating using a combination of the fact and reliability ratings from Ad Fontes Media and Media Bias/Fact Check.Follow See all of Interventional News news coverage in one place. Discover how Interventional News’s media bias informs their coverage and compare with thousands of other news outlets. We’ve discovered 84 headlines written by Interventional News during the past 3 months. The Ground News media bias check for Interventional News is . Scores are assigned by aggregating bias scores from Ad Fontes Media, Media Bias/Fact Check, and All Sides. Interventional News’s factuality rating is Unknown. Ground News calculates this rating using a combination of the fact and reliability ratings from Ad Fontes Media and Media Bias/Fact Check. Information about Interventional NewsWhere is Interventional News located?Interventional News's WebsiteMedia Bias RatingsDo you diasgree? Edit biasLearn more about Media Bias Ratings.FactualityAverage Factuality Rating: UnknownLearn more about Factuality Ratings.Top Interventional News NewsUnited States · United StatesXeltis announces US FDA Breakthrough Device Designation for aXess and first patient treated in US pivotal trial - Interventional NewsXeltis has today announced that the Center for Devices and Radiological Health (CDRH) of the US Food and Drug Administration (FDA) has granted aXess Breakthrough Device Designation status. aXess is Xeltis’ vascular access conduit, which enables the creation of a new, permanent, living vessel for haemodialysis vascular access. Concurrently, following investigational device exemption (IDE) approval from the US FDA, the first patient in aXess’ US-…See the StoryUnited States · United StatesGE Healthcare receives US FDA 510(k) clearance for Signa Magnus MRI scanner - Interventional NewsGE HealthCare has announced the US Food and Drug Administration (FDA) 510(k) clearance for its Signa Magnus magnetic resonance imaging (MRI) scanner. The 3-tesla (T) head-only scanner is designed to improve clinical imaging and neuroscience research, assisting in the detection of various oncological, neurological, and psychiatric conditions. Signa Magnus features a high-efficiency asymmetrical, gradient coil design. This design helps in achievin…See the StoryUnited States · United StatesHealionics’ STARgraft Receives FDA Breakthrough Device DesignationSEATTLE, WA, UNITED STATES, November 14, 2024 /EINPresswire.com/ -- Healionics Corporation, a developer of synthetic biomaterial-based medical devices, today announced that its STARgraft arteriovenous graft – designed to provide a safer and more reliable means of bloodstream access for kidney failure patients needing dialysis – has been granted Breakthrough Device designation by the FDA. The FDA’s Breakthrough Devices Program aims to identify im…See the StoryLatest News StoriesTopics Most Covered by Interventional NewsFDAWomen's RightsYaleUS EconomyEuropean UnionFDAWomen's RightsYaleSources Covering Similar TopicsCardiovascular NewsMedical Device NetworkEndovascular TodayMedical Device News MagazineMed-Tech Innovation | Latest news for the medical device industryCardiovascular NewsMedical Device NetworkEndovascular TodaySuggest a sourceLooking for a source we don't already have? Suggest one here.You've scrolled to the bottom of the feed, there are no more stories.
