Verilux VT31WW3
Verilux VT31WW3 is a Class I device made by Bear Down Consulting, listed in FDA GUDID since 17 May 2023 (UDI-DI 00768533140050), 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 | Number00768533140050 | Date17 May 2023 | StatusListed |
Official records
- AccessGUDID record 00768533140050
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- Withdrawn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
- VT31WW3
- Primary DI / UDI-DI
- 00768533140050
- 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
Similar devices
Other devices filed under FDA product code KZF (Device, Medical Examination, Ac Powered).
- LS100 HALOGEN EXAMINATION LIGHT, MODEL NO: 44100 by Welch Allyn, Inc.
- VITA LAMP, MODEL 0350 by Tensor Industries, Inc.
- NEVOSCOPE by Nizar A. Mullani
- WELCH ALLYN VIDEO EPISCOPE by Welch Allyn, Inc.
- MODEL 0450000, OPAL MEDICAL EXAM LIGHT by Burton Medical Products Corp.
- HALUX TASKLIGHT by Burton Medical Products Corp.
- ILLUMINATOR VIII ULTRA/SPOT by Medical Illumination, Inc.
- ILLUMINATOR III by Medical Illumination, Inc.
- Chromophare F300 CE2853075 CE 2853075 by Berchtold Holding GmbH
- HexaLux Light Wall Mount EXLWALL by STERIS CORPORATION