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Freshmint

FDA UDI

Class I (US FDA UDI)

by New World Imports, Inc.

Identity

Trade Name
Freshmint FDA UDI
Generic Name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI
Device Name
Freshmint® 2 oz Denture Adhesive, Zinc Free, Extra Strength holding power with easy open cap FDA UDI
Model / Reference
DA24 FDA UDI
Description
Freshmint® 2 oz Denture Adhesive, Zinc Free, Extra Strength holding power with easy open cap FDA UDI

Identifiers

Primary DI / UDI-DI
00085317005665 FDA UDI
FDA Product Code
KOO FDA UDI
GMDN Term
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3490 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

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: Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free

Freshmint by New World Imports, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
New World Imports, Inc.

Sources (1)

  • FDA UDI 9e47bee1-cd55-4990-b4e8-b0690955e46e 34 fields · synced Jun 1, 2026