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Henry Schein 1126716

by Henry Schein, Inc.

Henry Schein 1126716 is a device classified as Unclassified made by Henry Schein, Inc., listed in FDA GUDID since 21 Apr 2020 (UDI-DI 10304040029470), 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 Number10304040029470 UDI-DI Date21 Apr 2020ListedStatusListed 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  • Withdrawn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
Dental matrix band, reusable
Model / Ref / Catalog
1126716
Primary DI / UDI-DI
10304040029470
FDA product code
MVL
GMDN term
Dental matrix band, reusable
Device class
U
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental matrix band, reusable

Similar devices in this category

Other devices filed under Dental matrix band, reusable.

Other devices from Henry Schein, Inc.

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Properties

  • Prescription use
  • Combination product
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)