Orangecad Med GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Orangecad Med GmbH has 1 FDA 510(k) cleared medical devices. Based in Karlsruhe, DE.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Orangecad Med GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aclivi, LLC as regulatory consultant.
1 devices