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3M UNITEK CORPORATION

Last updated May 24, 2026

What 3M UNITEK CORPORATION makes

3M Unitek Corporation manufactures orthodontic products including metal and ceramic brackets, tubes, archwires, and metal bands. The company also produces progressive aligners, orthodontic pliers, and appliance relief materials.

These devices are classified as Class I and Class II medical devices and are listed in the FDA UDI database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of products does 3M Unitek Corporation manufacture?

3M Unitek Corporation specializes in the production of orthodontic equipment. Their product range includes metal and ceramic orthodontic brackets, orthodontic tubes, archwires, and metal bands. Additionally, the company manufactures orthodontic progressive aligners, specialized pliers, and appliance relief materials to support clinical orthodontic procedures.

Where is 3M Unitek Corporation based?

3M Unitek Corporation is based in the United States. This location serves as the primary base for the company's operations and the manufacturing of its orthodontic product lines.

How are the devices from 3M Unitek Corporation classified?

The medical devices manufactured by 3M Unitek Corporation are classified as either Class I or Class II devices. This classification system is used to determine the level of regulatory oversight required based on the risk profile and intended use of the specific orthodontic products.

Where can I find information regarding the registration of these devices?

The devices manufactured by 3M Unitek Corporation are listed in the FDA UDI database. This registry provides transparency and tracking for medical devices, ensuring that the company's products are documented according to regulatory requirements for unique device identification.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: mmm.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)423-4588
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 008256356

Catalogue (8379)

Page 6 of 168

Device	Model / Reference	Registries	Class	Status
3M™ Unitek™ OrthoForm™	300-905	FDA UDI	Class I	Active
APC™ II Victory Series™ Superior Fit	3069-5313	FDA UDI	Class II	Active
3M™ Victory Series™	953-280	FDA UDI	Class I	Active
APC™ II Victory Series™ Low Profile	3024-601	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-4320	FDA UDI	Class II	Active
3M™ Unitek™	163-380	FDA UDI	Class I	Active
3M™ Unitek™ Uni-Twin™	020-849	FDA UDI	Class I	Active
3m™	328-255	FDA UDI	Class II	Active
3M™ Unitek™	4297-924	FDA UDI	Class I	Active
3M™ Unitek™	020-714	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-607	FDA UDI	Class II	Active
3M™ Unitek™	4296-912	FDA UDI	Class I	Active
Clarity™ ADVANCED	006-362	FDA UDI	Class II	Active
APC™ II Unitek™ Gemini	3119-789	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5067-9404	FDA UDI	Class II	Active
3M™ Victory Series™	902-371	FDA UDI	Class I	Active
APC™ II Victory Series™ Low Profile	3024-874	FDA UDI	Class II	Active
APC™ PLUS Unitek™ Mini Uni-Twin	5020-465	FDA UDI	Class II	Active
APC™ PLUS Clarity™ SL	5007-420	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-780	FDA UDI	Class II	Active
Clarity™ SL	007-502	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	067-8271	FDA UDI	Class I	Active
3m™	9297-807	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-790	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-697	FDA UDI	Class II	Active
3M™ Unitek™ MBT™	119-690	FDA UDI	Class I	Active
Clarity™ Aligners	358-458	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	067-956	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™ MBT™	067-8731	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	067-8033	FDA UDI	Class I	Active
3M™ Unitek™ OrthoForm™	293-306	FDA UDI	Class I	Active
3M™ Victory Series™	902-172	FDA UDI	Class I	Active
3M™ Unitek™	119-635	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	061-252	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5067-8154	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5067-9782	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-595	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-122	FDA UDI	Class II	Active
3M™ Unitek™	020-701	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Superior Fit	4069-6424	FDA UDI	Class II	Active
3M™ Victory Series™	902-184	FDA UDI	Class I	Active
3M™ Unitek™	298-285	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	067-955	FDA UDI	Class I	Active
3M™ Incognito™	DE150003452	FDA UDI	Class I	Active
3M™ AlastiK™	406-312	FDA UDI	Class I	Active
APC™ II Victory Series™ Low Profile	3024-9831	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-903	FDA UDI	Class II	Active
3M™ Unitek™	4297-711	FDA UDI	Class I	Active
APC™ II Victory Series™ Superior Fit	3069-6324	FDA UDI	Class II	Active
3M™ Unitek™	297-871	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

There is one recall record for 3M Unitek Corporation initiated on 2024-11-26. The status of this record is listed as open and classified. The reason provided for the recall is an increase of complaints regarding bracket bond failures and skin irritation or blistering.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Nov 26, 2024	Z-0797-2025	—	open, classified	Due to an increase of complaints for bracket bond failures and skin irritation or blistering.