# Permedica

- Location (FDA's records): San Diego, CA
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: JWH (1)
- Predicates its devices cite: 7 (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
- Zimmer, Inc.: 3 (https://510kreport.com/company/zimmer)
- Medacta International S.A.: 1 (https://510kreport.com/company/medacta-international)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Consensus Orthopedics, Inc.: 1 (https://510kreport.com/company/consensus-orthopedics)
- Johnson & Johnson Professionals, Inc.: 1 (https://510kreport.com/company/johnson-johnson-professionals)

## Recent decisions
- K122975: GKS Prime Flex CR Total Knee System (Dec 20, 2012)

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