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Wolverine

FDA UDI

Class I (US FDA UDI)

by Kenmark Optical Co., Inc.

Identity

Trade Name
Wolverine FDA UDI
Generic Name
Prescription spectacles FDA UDI
Device Name
W045 Side Shield Clear Spectacle FDA UDI
Model / Reference
S045CL00 FDA UDI
Description
W045 Side Shield Clear Spectacle FDA UDI

Identifiers

Primary DI / UDI-DI
00715317119825 FDA UDI
FDA Product Code
HOI FDA UDI
GMDN Term
Prescription spectacles FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.5840 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

No

FDA UDI

Over-the-Counter

Yes

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

Wolverine by Kenmark Optical Co., Inc. — 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

Sources (1)

  • FDA UDI 8d45e5a4-303b-4cd4-9380-4116bdd5d0fe 34 fields · synced May 30, 2026