Verilux VT32WW3
Verilux VT32WW3 is a Class I device made by Bear Down Consulting, listed in FDA GUDID since 17 May 2023 (UDI-DI 00768533140043), 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 | Number00768533140043 | Date17 May 2023 | StatusListed |
Official records
- AccessGUDID record 00768533140043
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- Withdrawn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
- VT32WW3
- Primary DI / UDI-DI
- 00768533140043
- 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).
- HexaLux Ceiling Mount EXLCEIL by STERIS CORPORATION
- MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT by Meddev International Corp.
- EPISCOPE, MODEL 47300 by Welch Allyn, Inc.
- MEDICAL EXAMINATION LIGHTS by Burton Medical Products Corp.
- SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG by The Lighthouse For the Blind, Inc.
- Chromophare CH00000001 by Berchtold Holding GmbH
- WAVE FLUORESCENT MAGNIFIER by Burton Medical Products Corp.
- H 5100, H 5200, H 5300 by Rudolf Riester GmbH & Co. KG
- LIC 180 MEDICAL LAMPS by Lada Intl., Inc.
- VarioLux US MP00602 by Drägerwerk AG & Co. KGaA