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3M™ Clarity™

FDA UDI

Class II (US FDA UDI)

by 3m Unitek Corporation

Identity

Trade Name
3M™ Clarity™ FDA UDI
Generic Name
Orthodontic aligner auxiliary attachment kit FDA UDI
Device Name
3M™ Clarity™ Aligners AttachTemp Single Arch, 359-504 FDA UDI
Model / Reference
359-504 FDA UDI
Description
3M™ Clarity™ Aligners AttachTemp Single Arch, 359-504 FDA UDI

Identifiers

Catalog Number
359-504 FDA UDI
Primary DI / UDI-DI
00652221291066 FDA UDI
FDA Product Code
NXC FDA UDI
GMDN Term
Orthodontic aligner auxiliary attachment kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic aligner auxiliary attachment kit

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

Similar devices

Also classified as Orthodontic aligner auxiliary attachment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 440dca71-57f2-4676-b5ef-31e900473d8c 35 fields · synced May 30, 2026