XCELLARISPRO TWIST microneedling device— 510(k) K241790
Substantially EquivalentDermaroller GmbH
FDA 510(k) clearance K241790 for XCELLARISPRO TWIST microneedling device, Substantially Equivalent on 2025-03-06. Applicant: Dermaroller GmbH.
Clearance details
- Applicant
- Dermaroller GmbH
- Product code
- Code QAI
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wolfenbuettel, DE
Data sourced from openFDA. This site is unofficial and independent of the FDA.