Dermaroller GmbH
Dermaroller GmbH appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on March 6, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K241790 | XCELLARISPRO TWIST microneedling device | March 6, 2025 |