# Eufoton S.R.L.

- Location (FDA's records): Trieste, IT
- FDA decisions: 2 (2010–2026): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K092860: Lasemar 800, 1000, 1500 (2010), cited by 1

## Recent decisions
- K260489: LASEmaR 1500 (May 29, 2026)
- K092860: Lasemar 800, 1000, 1500 (Jul 16, 2010)

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