# Uroval

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: IKN (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- Motion Lab Systems, Inc.: 1 (https://510kreport.com/company/motion-lab-systems)
- The Prometheus Group: 1 (https://510kreport.com/company/prometheus-group)

## Recent decisions
- K083679: Uroval BRS System, Model BRS01; Telesis, Model PROMO1 (Sep 11, 2009)

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