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Henry Schein 5701364

by Henry Schein, Inc.

Henry Schein 5701364 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 26 Apr 2019 (UDI-DI 00304040108048), 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 Number00304040108048 UDI-DI Date26 Apr 2019ListedStatusListed 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  • Withdrawn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 post, preformed
Model / Ref / Catalog
5701364
Primary DI / UDI-DI
00304040108048
FDA product code
DZA
GMDN term
Root canal post, preformed
Device class
Class I
Regulation number
872.4130
GUDID distribution status
In Commercial Distribution

Related devices

Category: Root canal post, preformed

Similar devices in this category

Other devices filed under Root canal post, preformed.

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

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