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Build-It Light Cure

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Build-It Light Cure FDA UDI
Generic Name
Self-cured dental restorative composite resin FDA UDI
Device Name
Core Material; Single Doses; Sample; Refill FDA UDI
Model / Reference
N32UX FDA UDI
Description
Core Material; Single Doses; Sample; Refill FDA UDI

Identifiers

Primary DI / UDI-DI
10814978021427 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Self-cured dental restorative 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

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

Dimensions & Sizes

Size
Weight — 2.5 Gram FDA UDI

Category: Self-cured dental restorative composite resin

Build-It Light Cure by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-cured dental restorative composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 5c02b8e4-bd00-4ee8-ac47-0465ecfe5895 36 fields · synced Jun 8, 2026