Medical Device Manufacturer · IT , Trieste

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

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Eufoton S.R.L. has 2 FDA 510(k) cleared medical devices. Based in Trieste, IT.

Latest FDA clearance: May 2026. Active since 2010. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Eufoton S.R.L. Filter by specialty or product code using the sidebar.

Eufoton S.R.L. is one of 117 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

Eufoton S.R.L. — FDA 510(k) Products and Clearance History

2 devices

1-2 of 2