Ureteral Stent Company - FDA 510(k) Cleared Devices
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) cleared devices by Ureteral Stent Company
2 devices