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Freeze Away Max Plantar Wart Remover

FDA UDI

Class II (US FDA UDI)

by Scholl's Wellness Company

Identity

Trade Name
Freeze Away Max Plantar Wart Remover FDA UDI
Generic Name
Wart-removal cryogenic kit FDA UDI
Device Name
Cryogenic Wart remover for Plantar Warts FDA UDI
Model / Reference
90000384 FDA UDI
Description
Cryogenic Wart remover for Plantar Warts FDA UDI

Identifiers

Primary DI / UDI-DI
00888853003214 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Wart-removal cryogenic kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wart-removal cryogenic kit

Freeze Away Max Plantar Wart Remover by Scholl's Wellness Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wart-removal cryogenic kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scholl's Wellness Company

Sources (1)

  • FDA UDI d78bd275-8cbe-47b7-b5bb-c32a6f4a56d6 35 fields · synced Jun 6, 2026