Poiesis Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Poiesis Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Duette 100% Silicone Dual-Balloon, Temperature-Sensing Catheter
1
Total
1
Cleared
0
Denied
Poiesis Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Jupiter, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Poiesis Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Powers Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Poiesis Medical, LLC
1 devices