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Brush White #3 201103

by Cosmedent, Inc.

Brush White #3 201103 is a Class I device made by Cosmedent, Inc., listed in FDA GUDID since 26 Oct 2021 (UDI-DI D7792011031), 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 NumberD7792011031 UDI-DI Date26 Oct 2021ListedStatusListed 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  • Withdrawn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
Brush White #3
Generic name
Dental-professional prophylaxis brush, reusable
Model / reference
201103
Primary DI / UDI-DI
D7792011031
FDA product code
KXR
GMDN term
Dental-professional prophylaxis brush, reusable
Device class
Class I
Regulation number
872.3140
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental-professional prophylaxis brush, reusable

Similar devices

Other devices filed under FDA product code KXR (Applicator, Resin).

Other devices from Cosmedent, Inc.

See all devices from Cosmedent, Inc. →

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)