Zenith Thoraco+ Endovascular System Receives FDA Breakthrough Device Designationnews2022-04-01T09:15:53+00:00April 1st, 2022|Medical Device News Magazine, Uncategorized|
Aidoc Expands AI Service to X-ray, Receiving FDA 510(k) Clearance for Pneumothoraxnews2022-03-30T13:00:03+00:00March 30th, 2022|Medical Device News Magazine|
Cellmyx Announces FDA 510(k) Clearance for intelliFat® BOD™ (Ref.# K210528)news2022-03-29T12:39:32+00:00March 29th, 2022|Medical Device News Magazine|
FDA Seeks $8.4 Billion to Further Investments in Critical Public Health Modernization, Core Food and Medical Product Safety Programsnews2022-03-28T18:43:12+00:00March 28th, 2022|Medical Device News Magazine|
HLT Gains FDA Approval for Two TAVR Clinical Studiesnews2022-03-24T14:58:40+00:00March 24th, 2022|Medical Device News Magazine|
ArthroFree Wireless Camera System for Minimally Invasive Surgery Receives FDA Market Clearancenews2022-03-24T14:47:28+00:00March 24th, 2022|Medical Device News Magazine|
Cerus Endovascular Receives FDA 510(k) Clearance of its 027 Micro-catheternews2022-03-23T13:51:31+00:00March 23rd, 2022|Medical Device News Magazine|
Wision AI Expands U.S. Offerings to Combat Colorectal Cancer With Multiple Screening Toolsnews2022-03-22T15:22:13+00:00March 22nd, 2022|Medical Device News Magazine|
Solus Gold Embolization Device Receives FDA Clearancenews2022-03-22T11:19:06+00:00March 22nd, 2022|Medical Device News Magazine|
FDA Continues Co-sponsorship of MedCon Conference with AFDO/RAPS Healthcare Products Collaborativenews2022-03-17T17:02:53+00:00March 17th, 2022|Medical Device News Magazine|
