Orth Arch

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name: ORTH ARCH FDA UDI
Generic Name: Orthodontic metal band pusher FDA UDI
Device Name: BAND SEATER/ BITE STICK - AUTOCLAVABLE FDA UDI
Model / Reference: BAND SEATER/ BITE STICK FDA UDI
Description: BAND SEATER/ BITE STICK - AUTOCLAVABLE FDA UDI

Identifiers

Catalog Number: 800-0182 FDA UDI
Primary DI / UDI-DI: D90980001821 FDA UDI
FDA Product Code: DZN FDA UDI
GMDN Term: Orthodontic metal band pusher 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthodontic metal band pusher

Orth Arch by Ortho Arch Company Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Precision Dental Instruments — Precision Dental Instruments · Class I
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Quinelato — Schobell Industrial Ltda · Class I
Power Dental USA — Power Dental USA, Inc. · 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

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Manufacturer

Manufacturer: Ortho Arch Company Inc

Sources (1)

FDA UDI 60091c4d-defa-42e3-8fdd-84f671443852 35 fields · synced Jun 1, 2026