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Endo-Eze

FDA UDI

Class II (US FDA UDI)

by Ultradent Products, Inc.

Identity

Trade Name
Endo-Eze FDA UDI
Generic Name
Endodontic filling/sealing material FDA UDI
Device Name
Endo-Eze MTA FLOW Repair Cement Kit FDA UDI
Model / Reference
3980 FDA UDI
Description
Endo-Eze MTA FLOW Repair Cement Kit FDA UDI

Identifiers

Catalog Number
3980 FDA UDI
Primary DI / UDI-DI
00883205101594 FDA UDI
FDA Product Code
KIF FDA UDI
GMDN Term
Endodontic filling/sealing material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3820 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

Yes

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

Category: Endodontic filling/sealing material

Endo-Eze by Ultradent Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic filling/sealing material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c0d9be06-be39-4b9b-a224-af1d1eda22f5 36 fields · synced May 30, 2026