Erchonia CLX (Model # CFL)
510(k) K252574
Erchonia CLX (Model # CFL) is a Class II device made by Erchonia Corporation, cleared under FDA 510(k) K252574 on 15 Dec 2025, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK252574 | Date15 Dec 2025 | StatusActive |
Official records
- FDA 510(k) database K252574
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- OLI
- Device class
- Class II
- Regulation
- 21 CFR Part 878.5400
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K252574
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Erchonia CLX CFL | CFL / CFL | 00858985006391 | — | On the market |
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