Zynex Submits FDA Application for its Next Generation Fluid and Blood Volume Monitornews2022-01-03T14:41:52+00:00January 3rd, 2022|Medical Device News Magazine, Uncategorized|
Paragon 28, Inc. R3ACT™ Stabilization System Cleared by FDAnews2021-12-29T17:28:49+00:00December 29th, 2021|Medical Device News Magazine|
Nobel Biocare Receives FDA 510(k) Clearance for the Nobel Biocare N1™ Implant Systemnews2021-12-27T13:19:38+00:00December 27th, 2021|Medical Device News Magazine|
Coronavirus (COVID-19) Update: FDA Authorizes Additional Oral Antiviral for Treatment of COVID-19 in Certain Adultsnews2021-12-23T15:09:08+00:00December 23rd, 2021|Medical Device News Magazine|
OrganOx Receives FDA Approval for its Liver Normothermic Machine Perfusion Systemnews2021-12-20T15:38:49+00:00December 20th, 2021|Medical Device News Magazine|
MOWOOT earns FDA’s First-Ever ‘Breakthrough Device Designation’ for a Novel Non-Drug and Non-Invasive Therapy of Neurogenic Bowel Disordernews2021-12-17T12:15:22+00:00December 17th, 2021|Medical Device News Magazine|
MOWOOT earns FDA’s First-Ever ‘Breakthrough Device Designation’ for a Novel Non-Drug and Non-Invasive Therapy of Neurogenic Bowel Disordernews2021-12-17T12:15:22+00:00December 17th, 2021|Medical Device News Magazine|
Svelte Medical Systems Receives FDA Approval For SLENDER IDS® And DIRECT RX® Bioresorbable Coated Drug-Eluting Stent Systemsnews2021-12-14T15:56:55+00:00December 14th, 2021|Medical Device News Magazine|
Cooler Heads Receives FDA Clearance To Help Save Cancer Patients’ Hairnews2021-12-08T14:31:06+00:00December 8th, 2021|Medical Device News Magazine|
FDA In Brief: FDA Takes New Steps Aimed at Advancing Development of Individualized Medicines to Treat Genetic Diseasesnews2021-12-07T20:33:43+00:00December 7th, 2021|Medical Device News Magazine|
