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Encore

FDA UDI

Class II (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
Encore FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Encore Natural without Fluoride composite kit FDA UDI
Model / Reference
310077 FDA UDI
Description
Encore Natural without Fluoride composite kit FDA UDI

Identifiers

Primary DI / UDI-DI
00817051020556 FDA UDI
510(k) Number
K921174 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

Yes

FDA UDI

Category: Dental composite resin

Encore by Centrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI 2548e601-b2ff-4e01-bf89-18db2a521dd7 34 fields · synced Jun 1, 2026