Gruppo Europeo Ortodonzia Srl - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Gruppo Europeo Ortodonzia Srl has 1 FDA 510(k) cleared medical devices. Based in Rome, IT.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Gruppo Europeo Ortodonzia Srl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Donawa Lifescience Consulting Srl as regulatory consultant.
1 devices