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Repair Material

FDA UDI

Class II (US FDA UDI)

by American Tooth Industries

Identity

Trade Name
REPAIR MATERIAL FDA UDI
Generic Name
Dental acrylic resin FDA UDI
Device Name
REPAIR POWDER REG. PINK 7LB FDA UDI
Model / Reference
072-06-0014 FDA UDI
Description
REPAIR POWDER REG. PINK 7LB FDA UDI

Identifiers

Primary DI / UDI-DI
D772ATI0600140 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental acrylic 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: Dental acrylic resin

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

Similar devices

Also classified as Dental acrylic resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9de36224-4577-4318-ac17-1034a0e08eac 33 fields · synced May 30, 2026