Dmg Digital Enterprises SE - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dmg Digital Enterprises SE has 1 FDA 510(k) cleared medical devices. Based in Hamburg, DE.
Last cleared in 2021. Active since 2021. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dmg Digital Enterprises SE Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Delphi Medical Device Consulting, Inc. as regulatory consultant.
1 devices