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Og

FDA UDI

Class I (US FDA UDI)

by Zero G Eyewear

Identity

Trade Name
OG FDA UDI
Generic Name
Prescription spectacles FDA UDI
Model / Reference
Maiden Lane Arctic Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00840322904774 FDA UDI
FDA Product Code
HQZ FDA UDI
GMDN Term
Prescription spectacles FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5842 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Prescription spectacles

Og by Zero G Eyewear — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Prescription spectacles.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zero G Eyewear

Sources (1)

  • FDA UDI 30bf671f-3671-4da8-8313-776b8ea7a902 32 fields · synced May 31, 2026