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Henry Schein 9001586

by Henry Schein, Inc.

Henry Schein 9001586 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI H65890015861), 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 NumberH65890015861 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Henry Schein
Generic name
Light-cured dental restorative composite resin
Model / Ref / Catalog
9001586
Primary DI / UDI-DI
H65890015861
FDA product code
EBF
GMDN term
Light-cured dental restorative composite resin
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Light-cured dental restorative composite resin

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)