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.
510(k) submissions have been managed by Buchanan as regulatory consultant.
FDA 510(k) Regulatory Record - Dermaroller GmbH
1 devices