# Global Manufacturing Technology

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (2011–2013): 3 510(k) clearances
- Product codes: MEH (2), LZO (1)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 3 (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
- Wrightmedicaltechnologyinc: 2 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Aesculap Implant Systems, LLC: 1 (https://510kreport.com/company/aesculap-implant-systems)
- Aesculap Implant System, Inc.: 1 (https://510kreport.com/company/aesculap-implant-system)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Mayo Clinic: 1 (https://510kreport.com/company/mayo-clinic)
- Omni Life Science, Inc.: 1 (https://510kreport.com/company/omni-life-science)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)

## Firms that cite its devices most
- Signature Orthopaedics Pty, Ltd.: 1 (https://510kreport.com/company/signature-orthopaedics)
- Omnlife Science: 1 (https://510kreport.com/company/omnlife-science)

## Its most-cited devices
- K102172: Msa Hip System (2011), cited by 2
- K123782: Paragon Hip System (2013), cited by 1

## Recent decisions
- K123782: Paragon Hip System (Mar 14, 2013)
- K113107: Msa Hip System (Dec 15, 2011)
- K102172: Msa Hip System (Mar 1, 2011)

Source page: https://510kreport.com/company/global-manufacturing-technology