Campomats S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Campomats S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: 1NEED Pro
1
Total
1
Cleared
0
Denied
Campomats S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Riccione, IT.
Latest FDA clearance: Mar 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Campomats S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Whitelab S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - Campomats S.R.L.
1 devices