K253002
- 510(k) number
- K253002
- Device name
- SkinStylus SteriLock MicroSystem (MP1209SL)
- Applicant
- Esthetic Medical, Inc. CA · US
- Product code
- QAI — Powered Microneedle Device
- Decision date
- 2026-02-19
- Date received
- 2025-09-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K253002.pdf
Official FDA record: K253002
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.