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Renamel® Flowable Microhybrid

FDA UDI

Class II (US FDA UDI)

by Cosmedent, Inc.

Identity

Trade Name
Renamel® Flowable Microhybrid FDA UDI
Generic Name
Dental composite resin FDA UDI
Model / Reference
7011C3 FDA UDI

Identifiers

Catalog Number
7011C3 FDA UDI
Primary DI / UDI-DI
D7797011C30 FDA UDI
510(k) Number
K222435 FDA UDI
K980298 FDA UDI
FDA Product Code
EBD FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3310 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

Category: Dental composite resin

Renamel® Flowable Microhybrid by Cosmedent, 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

Manufacturer's product page: Renamel Microhybrid Composite

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cosmedent, Inc.

Sources (1)

  • FDA UDI 04af15ef-4f38-4ac0-b66e-9e21350efa21 34 fields · synced Jun 8, 2026