Dermaroller GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dermaroller GmbH has 1 FDA 510(k) cleared medical devices. Based in Wolfenbuettel, DE.
Latest FDA clearance: Mar 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dermaroller GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Dermaroller GmbH
1 devices