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Omni 24-42946

by Keystone Industries

Omni 24-42946 is a Class I device made by Keystone Industries, listed in FDA GUDID since 21 Jun 2024 (UDI-DI H6683524861), 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 NumberH6683524861 UDI-DI Date21 Jun 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Omni
Generic name
Dentifrice
Model / Ref / Catalog
24-42946
Primary DI / UDI-DI
H6683524861
FDA product code
EJR
GMDN term
Dentifrice
Device class
Class I
Regulation number
872.6030
GUDID distribution status
In Commercial Distribution

Other devices from Keystone Industries

See all devices from Keystone Industries →

Properties

  • Single use
  • Prescription use
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)