# Orthopedic Source, Inc.

- Location (FDA's records): Loomis, CA
- FDA decisions: 3 (2001–2006): 3 510(k) clearances
- Product codes: LPH (2), JDI (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (1 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
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Firms that cite its devices most
- Hayes Medical, Inc.: 1 (https://510kreport.com/company/hayes-medical)

## Its most-cited devices
- K022711: Modification to Avalon Cup System (2002), cited by 1
- K011887: Avalon Cup System (2001), cited by 1

## Recent decisions
- K061124: Orthopedic Source Press-Fit Hip (Jul 18, 2006)
- K022711: Modification to Avalon Cup System (Aug 26, 2002)
- K011887: Avalon Cup System (Dec 27, 2001)

Source page: https://510kreport.com/company/orthopedic-source