# Porex Medical

- Location (FDA's records): Fairburn, GA
- FDA decisions: 15 (1983–1987): 15 510(k) clearances
- Product codes: FWP (2), HPZ (1), KDG (1), FZE (1), GCY (1), HQX (1), FZZ (1), FZD (1), LCJ (1), LRC (1), FSE (1), ETN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Implantech Associates, Inc.: 1 (https://510kreport.com/company/implantech-associates)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Synthes (USA) Products, LLC: 1 (https://510kreport.com/company/synthes-usa-products)

## Its most-cited devices
- K832283: Medpar Surgical Implants (1984), cited by 2
- K863939: Porex (TM) Ear Prosthesis (1986), cited by 1

## Recent decisions
- K872791: Porex Nerve Locator (Oct 20, 1987)
- K873044: Porex Otology Instruments (Sep 4, 1987)
- K872947: Porex Quality Plastic Surgery Instruments (Aug 21, 1987)
- K863943: Porex (TM) Eye Sphere Implant (Feb 27, 1987)
- K863946: Porex (TM) Extra-Ocular Orbital Implant (Feb 27, 1987)
- K870257: Porex (TM) Silicone Surgical Implants for E.N.T. (Feb 24, 1987)
- K870154: Porex (TM) Tissue Expander (Feb 24, 1987)
- K870182: Porex (TM) Malar Implant (Feb 24, 1987)

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