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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 2 of 168

Device	Model / Reference	Registries	Class	Status
3M™ Unitek™ Uni-Twin™	020-956	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	068-861	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	066-5064	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	067-8163	FDA UDI	Class I	Active
3M™ Unitek™	4296-814	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-657	FDA UDI	Class II	Active
APC™ II Unitek™ Gemini	3119-773	FDA UDI	Class II	Active
APC™ II Victory Series™ Low Profile	3024-8711	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-682	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	068-8971B	FDA UDI	Class I	Active
3M™ Victory Series™	953-366	FDA UDI	Class I	Active
3M™ Victory Series™	952-386	FDA UDI	Class I	Active
APC™ II Unitek™ Mini Uni-Twin	3020-8540	FDA UDI	Class II	Active
APC™ II Victory Series™ V-Slot	3017-558	FDA UDI	Class II	Active
3M™ Unitek™ Uni-Twin™	020-475	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	067-830	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-896	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-981	FDA UDI	Class II	Active
3M™ Unitek™	4296-985	FDA UDI	Class I	Active
APC™ II Unitek™ Gemini	3119-668	FDA UDI	Class II	Active
APC™ PLUS Clarity™ ADVANCED	5006-153	FDA UDI	Class II	Active
3M™ Victory Series™	952-364	FDA UDI	Class I	Active
APC™ II Unitek™ Mini Uni-Twin	3020-517	FDA UDI	Class II	Active
APC™ II Unitek™ Mini Uni-Twin	3020-4230	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	067-8024B	FDA UDI	Class I	Active
APC™ PLUS Victory Series™ V-Slot	5017-8200	FDA UDI	Class II	Active
APC™ PLUS Clarity™ SL	5007-136	FDA UDI	Class II	Active
Clarity™ SL SmartClip™ SL3	007-113	FDA UDI	Class II	Active
APC™ PLUS Unitek™ Mini Uni-Twin	5020-564	FDA UDI	Class II	Active
APC™ PLUS SmartClip™ SL3	5004-3410	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-727	FDA UDI	Class II	Active
APC™ Flash-Free SmartClip™ SL3	4004-508	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	024-810	FDA UDI	Class I	Active
APC™ Flash-Free SmartClip™ SL3	4004-242	FDA UDI	Class II	Active
APC™ II Unitek™ Mini Uni-Twin	3020-513	FDA UDI	Class II	Active
3M™ Unitek™ Uni-Twin™	020-993	FDA UDI	Class I	Active
3M™ Victory Series™	951-406	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	068-962	FDA UDI	Class I	Active
APC™ PLUS Victory Series™ Low Profile	5024-604	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-425	FDA UDI	Class II	Active
3M™ Victory Series™	952-478	FDA UDI	Class I	Active
3M™ Unitek™	149-227	FDA UDI	Class I	Active
Clarity™ ADVANCED	006-216	FDA UDI	Class II	Active
3M™ Unitek™	4581-306	FDA UDI	Class I	Active
APC™ PLUS Unitek™ Mini Uni-Twin	5020-560	FDA UDI	Class II	Active
3M™ Unitek™	481-001	FDA UDI	Class I	Active
3M™ Victory Series™	955-157	FDA UDI	Class I	Active
APC™ PLUS Unitek™ Miniature Twin	5017-218	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	067-9673	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™ MBT™	067-97918B	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.