# Matrix Surgical Holdings, LLC/Matrix Surgical USA

- Location (FDA's records): Atlanta, GA
- FDA decisions: 2 (2014–2018): 2 510(k) clearances
- Product codes: JEY (1), KKY (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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 whose devices it cites most
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Matrix Surgical USA: 1 (https://510kreport.com/company/matrix-surgical-usa)
- Porex Surgical, Inc.: 1 (https://510kreport.com/company/porex-surgical)

## Recent decisions
- K180249: OmniPore DUROMAX Surgical Implants (Oct 11, 2018)
- K133046: Omnipore Customized Surgical Implants (May 14, 2014)

Source page: https://510kreport.com/company/matrix-surgical-holdings-matrix-surgical-usa