M&T S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
M&T S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: MTONE EVO (MTONE EVO), MT One, MT One Diamond
4
Total
4
Cleared
0
Denied
M&T S.R.L. has 4 FDA 510(k) cleared medical devices. Based in Rimini, IT.
Latest FDA clearance: Sep 2024. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by M&T S.R.L. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Endo Engineering S.R.L. and Endo Engineering.
FDA 510(k) Regulatory Record - M&T S.R.L.
4 devices