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Id Lightcure System Trans Gel Glaze

by Id Korea Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809896990851 UDI-DI Date14 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Id Lightcure System
Generic Name
Dental unfilled resin sealant/coating
Model / Reference
TRANS GEL GLAZE
Primary DI / UDI-DI
08809896990851
510(k) Number
FDA Product Code
EBD
GMDN Term
Dental unfilled resin sealant/coating
Device Class
Class II
Regulation Number
872.3310
GUDID distribution status
In Commercial Distribution
Size
Weight — 6 Gram

Related devices

Cleared under the same submission (K250804)

Show all (12)

Other devices from Id Korea Co., Ltd.

See all devices from Id Korea Co., Ltd. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No