# Lokki

- Location (FDA's records): Vienne, FR
- FDA decisions: 2 (1995–2000): 2 510(k) clearances
- Product codes: GEX (1), EBZ (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
- K994028: Flipo Xenon Curing Light (Jan 12, 2000)
- K952682: Lokki DT (Nov 14, 1995)

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