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Henry Schein 5702837

by Henry Schein, Inc.

Henry Schein 5702837 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 8 Apr 2022 (UDI-DI 10304040162511), 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 Number10304040162511 UDI-DI Date8 Apr 2022ListedStatusListed 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  • Withdrawn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
Henry Schein
Generic name
Basic manual toothbrush
Model / Ref / Catalog
5702837
Primary DI / UDI-DI
10304040162511
FDA product code
EFW
GMDN term
Basic manual toothbrush
Device class
Class I
Regulation number
872.6855
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic manual toothbrush

Similar devices

Other devices filed under FDA product code EFW (TOOTHBRUSH, MANUAL).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)