I.T.S. Group S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
I.T.S. Group S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: Stardust Med
1
Total
1
Cleared
0
Denied
I.T.S. Group S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Calderara Di Reno, IT.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by I.T.S. Group S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Endo Engineering S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - I.T.S. Group S.R.L.
1 devices