# Urosurge, Inc.

- Location (FDA's records): Coralville, IA
- FDA decisions: 4 (1998–2000): 3 510(k) clearances and 1 De Novo grant
- Product codes: FAD (3), NAM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- DEN000002: Urosurge Percutaneous Sans (Stoller Afferent Nerve Stimulator) Device (Feb 9, 2000)
- K992391: Urosurge Spiralflo Ureteral Stent (Aug 18, 1999)
- K981491: Urosurge Filastent Ureteral Stent (May 29, 1998)
- K981489: Urosurge Spirastent Plus Ureteral Stent (May 29, 1998)

Source page: https://510kreport.com/company/urosurge