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Build-It Light Cure N32UX

by Kerr Corporation

Build-It Light Cure N32UX is a Class II device made by Kerr Corporation, listed in FDA GUDID since 1 Aug 2016 (UDI-DI 10814978021427), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10814978021427 UDI-DI Date1 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Build-It Light Cure
Generic name
Self-cured dental restorative composite resin
Model / reference
N32UX
Primary DI / UDI-DI
10814978021427
FDA product code
EBF
GMDN term
Self-cured dental restorative composite resin
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution
Size
Weight — 2.5 Gram

Similar devices

Other devices filed under FDA product code EBF (MATERIAL, TOOTH SHADE, RESIN).

Other devices from Kerr Corporation

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Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)