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3M™ Unitek™

FDA UDI

Class I (US FDA UDI)

by 3m Unitek Corporation

Identity

Trade Name
3M™ Unitek™ FDA UDI
Generic Name
Orthodontic spring FDA UDI
Device Name
342-101 Unitek™ Edgewise Retraction Spring 10/Pk FDA UDI
Model / Reference
342-101 FDA UDI
Description
342-101 Unitek™ Edgewise Retraction Spring 10/Pk FDA UDI

Identifiers

Catalog Number
342-101 FDA UDI
Primary DI / UDI-DI
00652221071712 FDA UDI
FDA Product Code
ECO FDA UDI
GMDN Term
Orthodontic spring FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 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

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 spring

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

Similar devices

Also classified as Orthodontic spring.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dea713c6-d1ff-412d-91cd-6500abc0b4fa 35 fields · synced May 30, 2026