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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 lock FDA UDI
Device Name
3M™ Unitek™ Gurin Lock, 560-400, For Archwire .038/.045 in, 1/Pk FDA UDI
Model / Reference
560-400 FDA UDI
Description
3M™ Unitek™ Gurin Lock, 560-400, For Archwire .038/.045 in, 1/Pk FDA UDI

Identifiers

Catalog Number
560-400 FDA UDI
Primary DI / UDI-DI
00652221099198 FDA UDI
FDA Product Code
ECN FDA UDI
GMDN Term
Orthodontic lock 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 lock

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

Similar devices

Also classified as Orthodontic lock.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f2f3893-b354-45db-a391-4753ff2f6bbd 35 fields · synced May 30, 2026