# Aculux

- Location (FDA's records): Naples, FL
- FDA decisions: 2 (2000–2002): 2 510(k) clearances
- Names in FDA's records: Aculux (1); Aculux, Inc. (1)
- Product codes: FQP (1), FSW (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
- K013511: Xenalight Models # AX9125 (100-120V~); # AX9225 (220-240V~) (Feb 1, 2002)
- K001223: Aculux, Model AX3001, AX3002 (Jun 23, 2000)

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