K253765
- 510(k) number
- K253765
- Device name
- VANISH PRO
- Applicant
- Ddc Technologies, Inc. NY · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2026-04-22
- Date received
- 2025-11-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K253765.pdf
Official FDA record: K253765
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.