Artiness S.R.L is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Artiness S.R.L - FDA 510(k) Cleared Devices
Recent clearances: ARTICOR planner
1
Total
1
Cleared
0
Denied
Artiness S.R.L has 1 FDA 510(k) cleared medical devices. Based in Milan, IT.
Latest FDA clearance: Mar 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Artiness S.R.L Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Namsa as regulatory consultant.
FDA 510(k) Regulatory Record - Artiness S.R.L
1 devices