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Gradia® 002046

by Gc America Inc. 2 variants

Gradia 002046 is a dental composite resin (FDA Class II; FDA product code EBF, Material, tooth shade, resin) made by Gc America Inc., cleared under FDA 510(k) K023814 on 30 Jan 2003 and listed in FDA GUDID since 5 Aug 2022 (UDI-DI 14548161074155), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K023814

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14548161074155 UDI-DI Date5 Aug 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK023814 Date30 Jan 2003DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K023814 decided 30 Jan 2003 Active
  • FDA GUDID UDI-DI 14548161074155 listed 5 Aug 2022 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K023814
  2. Listed FDA GUDID 14548161074155

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Gradia®
Generic name
Dental composite resin
Model / Ref / Catalog
002046
Primary DI / UDI-DI
14548161074155
510(k) Number
FDA product code
EBF
GMDN term
Dental composite resin
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 2.4 Milliliter

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Properties

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