Eufoton S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Eufoton S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: LASEmaR 1500
2
Total
2
Cleared
0
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.
FDA 510(k) Regulatory Record - Eufoton S.R.L.
2 devices