Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: Millennium FDA UDI
Generic Name: Dental cheek retractor, professional, reusable FDA UDI
Device Name: Hargis Cheek Retractor FDA UDI
Model / Reference: 17-010147 FDA UDI
Description: Hargis Cheek Retractor FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776363222 FDA UDI
FDA Product Code: EIG FDA UDI
GMDN Term: Dental cheek retractor, professional, reusable 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: Dental cheek retractor, professional, reusable

Millennium by AVALIGN TECHNOLOGIES, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Dental cheek retractor, professional, reusable.

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STERLING — BENCO DENTAL SUPPLY CO. · Class I
GoldenDent — GoldenDent · Class I
Extraoral Cheek Retractors — ORTHO TECHNOLOGY, INC. · Class I
Extraoral Cheek Retractors — ORTHO TECHNOLOGY, INC. · 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: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI 69f36291-c14e-48a5-bd4c-71e4984d2c72 34 fields · synced May 30, 2026