# Arent Fox

- Location (FDA's records): Washington, DC
- FDA decisions: 4 (1994–1995): 4 510(k) clearances
- Product codes: EJI (1), KGD (1), KGO (1), HQC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K945843: Safety Plus (Jul 11, 1995)
- K944053: Natural Rubber Latex Surgeons Glove (Apr 25, 1995)
- K945583: Ocusystem (Art) (Feb 13, 1995)
- K944054: Powder Free Surgeon's Glove (Nov 17, 1994)

Source page: https://510kreport.com/company/arent-fox