# Aston Medical

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 3 (2011–2014): 3 510(k) clearances
- Product codes: KWS (1), PHX (1), LZO (1)
- Predicates its devices cite: 10 (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
- DePuy Orthopaedics, Inc.: 2 (https://510kreport.com/company/depuy-orthopaedics)
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)
- Tornier, Inc.: 1 (https://510kreport.com/company/tornier)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Plus Orthopedics: 1 (https://510kreport.com/company/plus-orthopedics)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Medacta International S.A.: 1 (https://510kreport.com/company/medacta-international)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Firms that cite its devices most
- Fournitures Hospitalieres Industrie: 1 (https://510kreport.com/company/fournitures-hospitalieres-industrie)

## Its most-cited devices
- K103251: Duocentric Reversed (2011), cited by 2

## Recent decisions
- K133462: Duocentric Reversed Shoulder Prosthesis (Feb 7, 2014)
- K111981: Tregor Dual Mobility Acetabular System (Oct 12, 2012)
- K103251: Duocentric Reversed (Oct 28, 2011)

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