# Portland Orthopaedics Pty., Ltd.

- Location (FDA's records): Stillwater, MN
- FDA decisions: 6 (2000–2007): 6 510(k) clearances
- Names in FDA's records: Portland Orthopaedics Pty. , Ltd. (5); Portland Orthopaedics Limited (1)
- Product codes: MEH (2), MAY (1), JDI (1), LPH (1), LZO (1)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 71 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Joint Medical Products Corp.: 3 (https://510kreport.com/company/joint-medical-products)
- Biomet, Inc.: 2 (https://510kreport.com/company/biomet)
- Metagen, LLC: 1 (https://510kreport.com/company/metagen)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Smith & Nephew Richards, Inc.: 1 (https://510kreport.com/company/smith-nephew-richards)

## Firms that cite its devices most
- Plus Orthopedics: 1 (https://510kreport.com/company/plus-orthopedics)
- Medacta International S.A.: 1 (https://510kreport.com/company/medacta-international)

## Its most-cited devices
- K063278: Portland Cobalt Chrome Femoral Head (2007), cited by 1
- K992815: The Margron Hip Replacement System (2000), cited by 1
- K061564: Portland Ceramic (Biolox-Forte) Femoral Head (2006), cited by 1

## Recent decisions
- K063278: Portland Cobalt Chrome Femoral Head (Jan 12, 2007)
- K061564: Portland Ceramic (Biolox-Forte) Femoral Head (Sep 1, 2006)
- K053417: M-Cor Hip Replacement System (Jul 20, 2006)
- K051844: Equator Plus Acetabular Cup System (Oct 7, 2005)
- K032641: Modification to: the Margron Hip Replacement System (Jan 20, 2004)
- K992815: The Margron Hip Replacement System (Feb 7, 2000)

Source page: https://510kreport.com/company/portland-orthopaedics