# Keri Medical SA

- Location (FDA's records): 1228 Plan-Les-Ouates
- FDA decisions: 2 (2022–2025): 1 510(k) clearance and 1 original PMA approval
- Product codes: SFA (1), KYJ (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
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)

## Recent decisions
- P240020: TOUCH® CMC 1 Prosthesis (Jul 10, 2025)
- K211385: KeriFlex® MCP and PIP Finger Joint Prostheses (Jul 27, 2022)

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