K251988
- 510(k) number
- K251988
- Device name
- Boston iFace (Boston iFace)
- Applicant
- Boston Aesthetics, Inc. DE · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-01-12
- Date received
- 2025-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251988.pdf
Official FDA record: K251988
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.