← Back to catalogue

Uvex

FDA UDI

Class I (US FDA UDI)

by Reliance Orthodontic Products, Inc.

Identity

Trade Name
UVEX FDA UDI
Generic Name
Phototherapy eye protector, reusable FDA UDI
Device Name
Uvex Skyper protective eyewear to protect eyes from powerful light sources being used in offices. These glasses can not be used with your prescription eyewear. FDA UDI
Model / Reference
SG FDA UDI
Description
Uvex Skyper protective eyewear to protect eyes from powerful light sources being used in offices. These glasses can not be used with your prescription eyewear. FDA UDI

Identifiers

Catalog Number
SG FDA UDI
Primary DI / UDI-DI
D798SG0 FDA UDI
FDA Product Code
HOY FDA UDI
GMDN Term
Phototherapy eye protector, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4750 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Phototherapy eye protector, reusable

Uvex by Reliance Orthodontic Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phototherapy eye protector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3d05d1f0-3aed-4536-b4b0-4d2e26e0fda3 36 fields · synced May 30, 2026