← Back to catalogue

Fusion

FDA UDI

Class II (US FDA UDI)

by Danville Materials, Llc

Identity

Trade Name
FUSION FDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
FUSION,TEMP,EXTREME,A3 FDA UDI
Model / Reference
FTXA3 FDA UDI
Description
FUSION,TEMP,EXTREME,A3 FDA UDI

Identifiers

Catalog Number
FTXA3 FDA UDI
Primary DI / UDI-DI
00816594023666 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

Yes

FDA UDI

Category: Temporary dental crown/bridge resin

Fusion by Danville Materials, Llc — 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

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

Manufacturer

Sources (1)

  • FDA UDI 542b283e-9a9b-4f8b-8f1e-77704175ec08 36 fields · synced Jun 1, 2026