← Back to catalogue

Mosaic

FDA UDI

Class II (US FDA UDI)

by Ultradent Products, Inc.

Identity

Trade Name
Mosaic FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Mosaic Singles A5 10pk FDA UDI
Model / Reference
4785 FDA UDI
Description
Mosaic Singles A5 10pk FDA UDI

Identifiers

Catalog Number
4785 FDA UDI
Primary DI / UDI-DI
00883205104595 FDA UDI
510(k) Number
K151094 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

Yes

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

Mosaic by Ultradent Products, 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

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

Manufacturer

Sources (1)

  • FDA UDI 83cd7eca-d484-42e7-a528-50c540a36fc3 37 fields · synced May 30, 2026