# Triopsy Medical, Inc.

- Location (FDA's records): Mankato, MN
- FDA decisions: 1 (2025–2025): 1 510(k) clearance
- Product codes: KNW (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
- Bip USA, Inc.: 2 (https://510kreport.com/company/bip-usa)

## Recent decisions
- K242228: Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01) (Jan 10, 2025)

Source page: https://510kreport.com/company/triopsy-medical