Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name: Henry Schein FDA UDI
Generic Name: Orthodontic pliers FDA UDI
Device Name: Maxima Hard Wire Cutter FDA UDI
Model / Reference: 9007602 FDA UDI
Description: Maxima Hard Wire Cutter FDA UDI

Identifiers

Catalog Number: 9007602 FDA UDI
Primary DI / UDI-DI: 00304040120323 FDA UDI
FDA Product Code: JEX FDA UDI
GMDN Term: Orthodontic pliers FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic pliers

Henry Schein by Henry Schein, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic pliers.

MIRABAY — MIRABAY ORTHODONTICS CORPORATION · Class I
Falcon — ORTHO TECHNOLOGY, INC. · Class I
J&J Instruments — J&J Instruments, LLC · Class I
FOR BENDING 45° WIRES — ZATTY INDUSTRIA COMERCIO IMPORTACAO E EXPORTACAO DE INSTRUMENTACAO CIRURGICA E ODONTOLOGICA LTDA · Class I
Orthopli — ORTHOPLI CORP. · Class I
Power Dental USA — Power Dental USA, Inc. · Class I
Triumph® — Ortho Organizers, Inc. · Class I
Pomee — POMEE CORPORATION · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Henry Schein, Inc.

Sources (1)

FDA UDI ee7f3605-f571-4e58-bc35-45d97e2d6c11 34 fields · synced Jun 1, 2026