Verilux VT39WW1
Verilux VT39WW1 is a Class I device made by Bear Down Consulting, listed in FDA GUDID since 17 May 2023 (UDI-DI 00817387026543), 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 | Number00817387026543 | Date17 May 2023 | StatusListed |
Official records
- AccessGUDID record 00817387026543
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Verilux
- Generic name
- Neurological visible-light phototherapy unit, home-use
- Model / reference
- VT39WW1
- Primary DI / UDI-DI
- 00817387026543
- FDA product code
- KZF
- GMDN term
- Neurological visible-light phototherapy unit, home-use
- Device class
- Class I
- Regulation number
- 880.6320
- GUDID distribution status
- In Commercial Distribution
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