# Porex Technologies Corp.

- Location (FDA's records): Fairburn, GA
- FDA decisions: 2 (1992–1997): 2 510(k) clearances
- Product codes: MQU (1), FWP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (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 that cite its devices most
- Porex Surgical, Inc.: 3 (https://510kreport.com/company/porex-surgical)
- Ceremed, Inc.: 2 (https://510kreport.com/company/ceremed)
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)
- Hohenstein Enterprises, Inc.: 1 (https://510kreport.com/company/hohenstein-enterprises)
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)
- Integrated Orbital Implants, Inc.: 1 (https://510kreport.com/company/integrated-orbital-implants)
- Matrix Surgical USA: 1 (https://510kreport.com/company/matrix-surgical-usa)
- Poriferous, LLC: 1 (https://510kreport.com/company/poriferous)

## Its most-cited devices
- K922489: Medpor Surg Implant Material:Prefor Cran/Fac Impla (1992), cited by 9
- K971583: Medpor Ocular Screw and Acceossories (1997), cited by 2

## Recent decisions
- K971583: Medpor Ocular Screw and Acceossories (Jun 30, 1997)
- K922489: Medpor Surg Implant Material:Prefor Cran/Fac Impla (Sep 2, 1992)

Source page: https://510kreport.com/company/porex-technologies