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Hexa CU-2011

by Hexa Dental

Hexa CU-2011 is a Class II device made by Hexa Dental, listed in FDA GUDID since 28 Mar 2023 (UDI-DI 10850023750768), 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 Number10850023750768 UDI-DI Date28 Mar 2023ListedStatusListed 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  • Withdrawn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
Hexa
Generic name
Dental composite resin kit
Model / Ref / Catalog
CU-2011
Primary DI / UDI-DI
10850023750768
FDA product code
EBF
GMDN term
Dental composite resin kit
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental composite resin kit

Other devices from Hexa Dental

See all devices from Hexa Dental →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)