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3m™

FDA UDI

Class II (US FDA UDI)

by 3m Unitek Corporation

Identity

Trade Name
3M™ FDA UDI
Generic Name
Orthodontic extraoral headgear FDA UDI
Device Name
Unitek(TM) Series 5 Facebow Short Size 5 .045 Diameter Ea FDA UDI
Model / Reference
328-252 FDA UDI
Description
Unitek(TM) Series 5 Facebow Short Size 5 .045 Diameter Ea FDA UDI

Identifiers

Catalog Number
328-252 FDA UDI
Primary DI / UDI-DI
00652221070135 FDA UDI
FDA Product Code
DZB FDA UDI
GMDN Term
Orthodontic extraoral headgear FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic extraoral headgear

3m™ by 3m Unitek Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic extraoral headgear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa2da615-964c-4cbf-902a-6044b03bc212 35 fields · synced May 30, 2026