Ureteral Stent Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ureteral Stent Company - FDA 510(k) Cleared Devices
Recent clearances: RELIEF™ Ureteral Stent Kit, RELIEF Ureteral Stent Kit
2
Total
2
Cleared
0
Denied
Ureteral Stent Company has 2 FDA 510(k) cleared medical devices. Based in Chagrin Falls, US.
Latest FDA clearance: Mar 2024. Active since 2022. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ureteral Stent Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ureteral Stent Company
2 devices