# Phoenix Bioengineering, Inc.

- Location (FDA's records): Bridgeport, PA
- FDA decisions: 3 (1991–1993): 3 510(k) clearances
- Product codes: GXR (1), KOB (1), HXA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)

## Its most-cited devices
- K913490: Phoenix Burr Hole Button, Burr 1 (1992), cited by 1

## Recent decisions
- K930125: Phoenix Bone Screws PBS-Type Series (Dec 30, 1993)
- K913490: Phoenix Burr Hole Button, Burr 1 (Jan 13, 1992)
- K904434: Sexton Cystotomy Urine Pump (SCUP2) (Feb 1, 1991)

Source page: https://510kreport.com/company/phoenix-bioengineering