# Poriferous, LLC

- Location (FDA's records): Newnan, GA
- FDA decisions: 2 (2014–2016): 2 510(k) clearances
- Product codes: FWP (1), KKY (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (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
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Porex Technologies Corp.: 1 (https://510kreport.com/company/porex-technologies)
- Matrix Surgical USA: 1 (https://510kreport.com/company/matrix-surgical-usa)

## Firms that cite its devices most
- Ceremed, Inc.: 1 (https://510kreport.com/company/ceremed)

## Its most-cited devices
- K140437: SU-Por Surgical Implant (2014), cited by 2

## Recent decisions
- K152463: SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant (Jan 20, 2016)
- K140437: SU-Por Surgical Implant (Jun 13, 2014)

Source page: https://510kreport.com/company/poriferous