Embolx, Inc. is one of 16484 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Embolx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Soldier Microcatheter, Sniper Infusion Catheter with Balloon Occlusion, Occlusion Balloon Catheter
3
Total
3
Cleared
0
Denied
Embolx, Inc. has 3 FDA 510(k) cleared medical devices. Based in Los Altos, US.
Latest FDA clearance: Feb 2024. Active since 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Embolx, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Coombs Medical Device Consulting and Third Party Review Group, LLC.
FDA 510(k) Regulatory Record - Embolx, Inc.
3 devices