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Henry Schein 1062552

by Henry Schein, Inc.

Henry Schein 1062552 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 21 Aug 2020 (UDI-DI 00304040120699), 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 Number00304040120699 UDI-DI Date21 Aug 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  • Withdrawn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
Orthodontic appliance system, bonded
Model / Ref / Catalog
1062552
Primary DI / UDI-DI
00304040120699
FDA product code
DYJ
GMDN term
Orthodontic appliance system, bonded
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthodontic appliance system, bonded

Similar devices

Other devices filed under FDA product code DYJ (RETAINER, SCREW EXPANSION, ORTHODONTIC).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)