Ureteral Stent Company

Ureteral Stent Company holds 2 FDA 510(k) medical device clearances, first cleared 2022, most recent 2024.

Top product codes for Ureteral Stent Company

FAD — Gastroenterology, Urology2 devices

Recent clearances by Ureteral Stent Company

K232920 — RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmCode FAD·2024-03-22
K213444 — RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmCode FAD·2022-03-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.