Orth Arch

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name: ORTH ARCH FDA UDI
Generic Name: Orthodontic ligature director FDA UDI
Device Name: LITE 3/8' DBL ENDED LIGATURE DIRECTOR FDA UDI
Model / Reference: DBL ENDED LIGATURE DIRECTOR FDA UDI
Description: LITE 3/8' DBL ENDED LIGATURE DIRECTOR FDA UDI

Identifiers

Catalog Number: 800-062W FDA UDI
Primary DI / UDI-DI: D909800062W1 FDA UDI
FDA Product Code: DZN FDA UDI
GMDN Term: Orthodontic ligature director 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 ligature director

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

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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 65a5c69f-ea1b-4125-b722-b0a70ac97c3f 35 fields · synced Jun 6, 2026