Medinice S.A. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Medinice S.A. has 1 FDA 510(k) cleared medical devices. Based in Warsaw, PL.
Latest FDA clearance: Feb 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medinice S.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept as regulatory consultant.
1 devices