WebApr 12, 2024 · Magnolia Medical Technologies has received the US Food and Drug Administration (FDA) 510 (k) approval for 19 new configurations within its Steripath Micro … WebApr 14, 2024 · Philips clarified on Friday that 2.2 million devices it has repaired or replaced in a major recall of respiratory devices are actually in the hands of patients in the United States. The Dutch healthcare equipment maker issued a statement clarifying progress of the recall program underway since 2024after the FDA issued a statement on April 13 saying …
FDA Industry Systems
WebMar 3, 2024 · To search for FDA-approved or FDA-cleared products by device name or company name: Go to the Devices@FDA Database . In the Enter a search term in the … Web1 day ago · The FDA cleared iTrack Advance for microcatheterization and viscodilation to reduce intraocular pressure (IOP). It treats adult patients with primary open-angle … flaggers jobs az show low
Are There "FDA Registered" or "FDA Certified" Medical Devices?
WebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique … Web2 days ago · April 11, 2024 By Sean Whooley. [Image from Moximed] Moximed announced that the FDA granted marketing authorization for its Misha knee system for treating knee osteoarthritis (OA). Misha, an ... WebThe record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. flaggers in wigan