← Back to catalogue

Unifast™

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
UNIFAST™ FDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
UNIFAST™LC 2 x 14.7 mL liquid btl FDA UDI
Model / Reference
000368 FDA UDI
Description
UNIFAST™LC 2 x 14.7 mL liquid btl FDA UDI

Identifiers

Catalog Number
000368 FDA UDI
Primary DI / UDI-DI
D0470003681 FDA UDI
510(k) Number
K890829 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Temporary dental crown/bridge resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 14.7 Milliliter FDA UDI

Category: Temporary dental crown/bridge resin

Unifast™ by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary dental crown/bridge resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI 5cbc5ae8-b5db-4f3d-88d5-787f4bc2a304 37 fields · synced May 30, 2026