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3M™ AlastiK™

FDA UDI

Class I (US FDA UDI)

by 3m Unitek Corporation

Identity

Trade Name
3M™ AlastiK™ FDA UDI
Generic Name
Orthodontic archwire/bracket ligature FDA UDI
Device Name
3M™ AlastiK™ QuiK-StiK™ Ligatures, 406-417, A-1, Clear, 60/Stick, 17/Pk FDA UDI
Model / Reference
406-417 FDA UDI
Description
3M™ AlastiK™ QuiK-StiK™ Ligatures, 406-417, A-1, Clear, 60/Stick, 17/Pk FDA UDI

Identifiers

Catalog Number
406-417 FDA UDI
Primary DI / UDI-DI
00652221075215 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic archwire/bracket ligature 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic archwire/bracket ligature

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

Similar devices

Also classified as Orthodontic archwire/bracket ligature.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 96f25a33-174a-4847-9230-d0aed5dd3c13 35 fields · synced May 29, 2026