Dermalux Flex MD
by Aesthetic Technology, Ltd. 2 variants
Dermalux Flex MD (1000053) is a Class II device made by Aesthetic Technology, Ltd., listed in FDA GUDID since 2 Sep 2025 (UDI-DI 05060762460028), registry data as of 23 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 | Number05060762460028 | Date2 Sep 2025 | StatusListed |
Official records
- AccessGUDID record 05060762460028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Dermalux
- Generic name
- Blue/red/infrared phototherapy lamp
- Model / Ref / Catalog
- Flex MD, 1000053
- Primary DI / UDI-DI
- 05060762460028
- FDA product code
- GEX, ILY
- GMDN term
- Blue/red/infrared phototherapy lamp
- Device class
- Class II
- Regulation number
- 878.4810, 890.5500
- GUDID distribution status
- In Commercial Distribution
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