OG Doheny Dr Onyx
OG Doheny Dr Onyx is a Class I device made by Zero G Eyewear, listed in FDA GUDID since 28 Feb 2023 (UDI-DI 00840322903562), 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 | Number00840322903562 | Date28 Feb 2023 | StatusListed |
Official records
- AccessGUDID record 00840322903562
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Og
- Generic name
- Prescription spectacles
- Model / reference
- Doheny Dr Onyx
- Primary DI / UDI-DI
- 00840322903562
- FDA product code
- HQZ
- GMDN term
- Prescription spectacles
- Device class
- Class I
- Regulation number
- 886.5842
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HQZ (Frame, Spectacle).
- DAELIM CORP. EYE WEAR MODEL by Daelim Corp.
- SPECTACLE FRAME by Australian Optical Co., Inc.
- FRAME, SPECTACLE by Swank Plus, Ltd.
- EYEGLASS FRAMES by Logo Paris, Inc.
- MILITARY PRESCRIPTION FRAME by Halo Optical Products, Inc.
- GLASS FRAMES & COMPONENT PARTS by Anamar
- SPECTACLE FRAMES by Euro Frame Design, Inc.
- OMYL -ARDE- SPECTACLE FRAME by I.J. Langleb, Ltd.
- OPTICAL FRAMES by Ramada Optics, Inc.
- SPECTACLE FRAMES (V.I.P. INT'L) by Continental Optical Imports