Iluminage HU-FG01751
Iluminage HU-FG01751 is a Class II device made by Tanda Beauty Canada, Inc, listed in FDA GUDID since 10 Jul 2017 (UDI-DI 00806248007296), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00806248007296 | Date10 Jul 2017 | StatusListed |
Official records
- AccessGUDID record 00806248007296
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Iluminage
- Generic name
- Cosmetic red-light phototherapy system, home-use
- Model / reference
- HU-FG01751
- Primary DI / UDI-DI
- 00806248007296
- FDA product code
- OHS
- GMDN term
- Cosmetic red-light phototherapy system, home-use
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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