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Henry Schein 1024971

by Henry Schein, Inc.

Henry Schein 1024971 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 28 Dec 2020 (UDI-DI 10304040058821), 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 Number10304040058821 UDI-DI Date28 Dec 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  • Withdrawn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
Root canal irrigation blunt needle
Model / Ref / Catalog
1024971
Primary DI / UDI-DI
10304040058821
FDA product code
DZM
GMDN term
Root canal irrigation blunt needle
Device class
Class I
Regulation number
872.4730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Root canal irrigation blunt needle

Similar devices

Other devices filed under FDA product code DZM (NEEDLE, DENTAL).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

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