Mojo

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name: Mojo FDA UDI
Generic Name: Dental cement trial FDA UDI
Device Name: Veneer Cement; Syringe; Try-In-Gel; Clear FDA UDI
Model / Reference: N06AC FDA UDI
Description: Veneer Cement; Syringe; Try-In-Gel; Clear FDA UDI

Identifiers

Primary DI / UDI-DI: 00814978020201 FDA UDI
FDA Product Code: EMA FDA UDI
GMDN Term: Dental cement trial FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3275 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Weight — 1.6 Gram FDA UDI

Category: Dental cement trial

Mojo by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Kerr Corporation

Sources (1)

FDA UDI 338f1eee-49cb-445d-82c2-2dde1f3a92ae 36 fields · synced Jun 8, 2026