Dmg Digital Enterprises SE is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Dmg Digital Enterprises SE - FDA 510(k) Cleared Devices
Recent clearances: LuxaPrint Ortho Plus
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.
FDA 510(k) Regulatory Record - Dmg Digital Enterprises SE
1 devices