# Medpac

- Location (FDA's records): Valencia, CA
- FDA decisions: 3 (1991–1995): 3 510(k) clearances
- Product codes: HRS (1), HWC (1), JDS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- TriMed, Inc.: 4 (https://510kreport.com/company/trimed)
- Tri-Med, Inc.: 2 (https://510kreport.com/company/tri-med)
- GM Dos Reis Industria e Comercio Ltda.: 1 (https://510kreport.com/company/gm-dos-reis-industria-e-comercio)
- Skeletal Dynamics, Inc.: 1 (https://510kreport.com/company/skeletal-dynamics)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)

## Its most-cited devices
- K951303: SFC (1995), cited by 6
- K951302: Small Fragment Plates and Screws (1995), cited by 3

## Recent decisions
- K951303: SFC (Jun 27, 1995)
- K951302: Small Fragment Plates and Screws (May 5, 1995)
- K903697: Hawaiian Supracondylar Plate (Jan 15, 1991)

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