Nx3

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name: NX3 FDA UDI
Generic Name: Dental cement trial FDA UDI
Device Name: Try-In Gel; Syringe; Bleach; Refill FDA UDI
Model / Reference: 33660 FDA UDI
Description: Try-In Gel; Syringe; Bleach; Refill FDA UDI

Identifiers

Catalog Number: 33660 FDA UDI
Primary DI / UDI-DI: 00841396105166 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 — 3 Gram FDA UDI

Category: Dental cement trial

Nx3 by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental cement trial.

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G-CEM LinkForce™ — Gc America Inc. · Class II
eCement Try-In Paste — BISCO INC. · Class I
Choice 2 Try-In Paste — BISCO INC. · Class II
Choice 2 Try-In Paste — BISCO INC. · Class I
Superdent® Pressure Indicator Paste — Dentsply International · Class I

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 0fa40d49-d3ea-4b8c-a495-11830fb2af39 37 fields · synced Jun 8, 2026