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Denture Base

FDA UDI

Class II (US FDA UDI)

by American Tooth Industries

Identity

Trade Name
DENTURE BASE FDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
DENTURE BASE 4 OZ SAMPLE M/FLASK FDA UDI
Model / Reference
072-04-0204 FDA UDI
Description
DENTURE BASE 4 OZ SAMPLE M/FLASK FDA UDI

Identifiers

Primary DI / UDI-DI
D772ATI0402040 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Temporary dental crown/bridge resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Temporary dental crown/bridge resin

Denture Base by American Tooth Industries — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary dental crown/bridge resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2711cac8-fc9f-4a82-bd5c-df94e735a3be 33 fields · synced Jun 8, 2026