Artiness S.R.L - FDA 510(k) Cleared Devices

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.