Device details
FDA 510(k) registration fields
- K number
- K253245
- Device name
- Boston 2910 (Boston 2910)
- Company
- Boston Aesthetics, Inc.
- Country / region
- United States(US)
- Product code
- GEX
- Device class
- Class 2
- Regulation number
- 21 CFR 878.4810
- Date received
- 2025-09-29
- Decision date
- 2026-05-21
- Submission type
- Traditional
