# Ureteral Stent Company

- Location (FDA's records): Chagrin Falls, OH
- FDA decisions: 2 (2022–2024): 2 510(k) clearances
- Product codes: FAD (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Dornier Medtech America, Inc.: 1 (https://510kreport.com/company/dornier-medtech-america)

## Firms that cite its devices most
- Shenzhen Trious Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-trious-medical-technology)

## Its most-cited devices
- K213444: RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm (2022), cited by 2

## Recent decisions
- K232920: RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm (Mar 22, 2024)
- K213444: RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm (Mar 17, 2022)

Source page: https://510kreport.com/company/ureteral-stent