Dreve Denatmid GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dreve Denatmid GmbH has 1 FDA 510(k) cleared medical devices. Based in Nordrhein-Westfalen, DE.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Dreve Denatmid GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bqc Consulting, LLC as regulatory consultant.
1 devices