K251699
- 510(k) number
- K251699
- Device name
- The Botticelli (Model: Athena)
- Applicant
- Bellamia Technologies, Inc. FL · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2025-10-08
- Date received
- 2025-06-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K251699.pdf
Official FDA record: K251699
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.