# Urometrics, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 3 (1997–2000): 2 510(k) clearances and 1 De Novo grant
- Product codes: NBV (1), LIL (1), IYN (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
- Dacomed Corp.: 1 (https://510kreport.com/company/dacomed)
- Specs USA, Inc.: 1 (https://510kreport.com/company/specs-usa)

## Recent decisions
- DEN000006: Eros-Clitoral Therapy Device (CTD) (Apr 28, 2000)
- K980627: Neva System (Apr 7, 1998)
- K971790: Knoll/Midus (Male Impotence Diagnostic Ultrasonic System) (Dec 17, 1997)

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