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Benda Brush 430007

by Centrix, Inc.

Benda Brush 430007 is a Class I device made by Centrix, Inc., listed in FDA GUDID since 29 Dec 2023 (UDI-DI 00817051023496), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817051023496 UDI-DI Date29 Dec 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  • Withdrawn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
Benda Brush
Generic name
Dental material application tool, single-use
Model / reference
430007
Primary DI / UDI-DI
00817051023496
FDA product code
KXR
GMDN term
Dental material application tool, single-use
Device class
Class I
Regulation number
872.3140
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental material application tool, single-use

Similar devices in this category

Other devices filed under Dental material application tool, single-use.

Other devices from Centrix, Inc.

See all devices from Centrix, Inc. →

Properties

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