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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 3 of 168

Device	Model / Reference	Registries	Class	Status
3M™ Incognito™	DE150004542	FDA UDI	Class I	Active
APC™ PLUS Clarity™ ADVANCED	5006-109	FDA UDI	Class II	Active
APC™ II Unitek™ Mini Uni-Twin	3020-9620	FDA UDI	Class II	Active
3M™ Unitek™	160-259	FDA UDI	Class I	Active
APC™ PLUS Victory Series™ V-Slot	5017-814	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-548	FDA UDI	Class II	Active
3M™ Unitek™ Uni-Twin™	020-514	FDA UDI	Class I	Active
3M™ Unitek™	404-226	FDA UDI	Class I	Active
APC™ II Victory Series™ Superior Fit	3069-5224	FDA UDI	Class II	Active
Clarity™ ADVANCED	006-146	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	024-8110	FDA UDI	Class I	Active
Clarity™ SL	007-549	FDA UDI	Class II	Active
3M™ Unitek™	9293-894	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	068-874	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-752	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-614	FDA UDI	Class II	Active
APC™ PLUS Victory Series™ Low Profile	5024-892	FDA UDI	Class II	Active
APC™ II Unitek™ Gemini	3119-616	FDA UDI	Class II	Active
3M™ Unitek™ Uni-Twin™	020-850	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5067-97648	FDA UDI	Class II	Active
APC™ II SmartClip™ SL3	3004-3490	FDA UDI	Class II	Active
3m™	415-060	FDA UDI	Class II	Active
APC™ II Victory Series™ Low Profile	3024-7960	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-6210	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-685	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	067-950	FDA UDI	Class I	Active
3M™ Unitek™	803-573	FDA UDI	Class I	Active
APC™ II Unitek™ Gemini	3027-324	FDA UDI	Class II	Active
APC™ II Clarity™ ADVANCED	3006-226	FDA UDI	Class II	Active
APC™ II SmartClip™ SL3	3004-410	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-511	FDA UDI	Class II	Active
3M™ Unitek™ Uni-Twin™	020-938	FDA UDI	Class I	Active
3M™ Unitek™	298-375	FDA UDI	Class I	Active
Clarity™ SL	007-550	FDA UDI	Class II	Active
3M™ Unitek™	9296-610	FDA UDI	Class I	Active
3M™ Victory Series™	957-155	FDA UDI	Class I	Active
3M™ Unitek™ OrthoForm™	300-935	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-605	FDA UDI	Class II	Active
3M™ Unitek™	900-753	FDA UDI	Class I	Active
3M™ Unitek™	4585-3045	FDA UDI	Class I	Active
APC™ Flash-Free Clarity™ SL	4007-151	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5058-802	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-7910	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-6990	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-805	FDA UDI	Class II	Active
3M™ Unitek™	298-486	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	068-812	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	067-917	FDA UDI	Class I	Active
APC™ PLUS Victory Series™ Low Profile	5024-126	FDA UDI	Class II	Active
3M™ Unitek™	4296-809	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.