Medical Device Manufacturer · IT , Trieste

Eufoton S.R.L. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Recent clearances: LASEmaR 1500, LASEMAR 800, 1000, 1500

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Eufoton S.R.L. General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared May 29, 2026

General & Plastic Surgery · 105d

Cleared Jul 16, 2010

LASEMAR 800, 1000, 1500

General & Plastic Surgery · 302d