Verilux VT43CG3
Verilux VT43CG3 is a Class I device made by Bear Down Consulting, listed in FDA GUDID since 17 May 2023 (UDI-DI 00817387025805), 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 | Number00817387025805 | Date17 May 2023 | StatusListed |
Official records
- AccessGUDID record 00817387025805
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- Withdrawn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
- VT43CG3
- Primary DI / UDI-DI
- 00817387025805
- 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).
- ILLUMINATOR III by Medical Illumination, Inc.
- Chromophare F300 CE2853075 CE 2853075 by Berchtold Holding GmbH
- HexaLux Light Wall Mount EXLWALL by STERIS CORPORATION
- AC-POWERED MEDICAL EXAMINATION LIGHT by Welch Allyn, Inc.
- HALOGEN EXAM. LITE #48400 by Welch Allyn, Inc.
- TINY HALOGEN EXAM LIGHT by JEDMED Instrument Company
- MODEL 0183010, PEARL MEDICAL EXAM LIGHT by Burton Medical Products Corp.
- ILLUMINATOR VII MINI/SPOT LIGHT by Medical Illumination, Inc.
- MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION by Meddev International Corp.
- HexaLux Light Mobile EXLMBWB by STERIS CORPORATION