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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 1 of 168

Device	Model / Reference	Registries	Class	Status
APC™ PLUS Victory Series™	5017-694	FDA UDI	Class II	Active
3M™ Unitek™	163-457	FDA UDI	Class I	Active
APC™ PLUS Victory Series™ Low Profile	5024-8130	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5067-8044	FDA UDI	Class II	Active
3M™ Victory Series™	953-380	FDA UDI	Class I	Active
Clarity™ ADVANCED	006-361	FDA UDI	Class II	Active
3M™ Victory Series™	905-250	FDA UDI	Class I	Active
3M™ Victory Series™	953-166	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™ MBT™	024-890	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™ MBT™	066-4071	FDA UDI	Class I	Active
3M™ Unitek™ MBT™	119-613	FDA UDI	Class I	Active
Clarity™ ADVANCED	006-223	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-913	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	068-990	FDA UDI	Class I	Active
APC™ II Level Anchorage™	3017-767	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-6190	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	066-5071	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-873	FDA UDI	Class II	Active
APC™ PLUS Clarity™ ADVANCED	5006-151	FDA UDI	Class II	Active
APC™ Flash-Free Clarity™ ADVANCED	4006-306	FDA UDI	Class II	Active
APC™ II Victory Series™	3058-802	FDA UDI	Class II	Active
APC™ II Victory Series™ V-Slot	3017-935	FDA UDI	Class II	Active
APC™ II SmartClip™ SL3	3004-104	FDA UDI	Class II	Active
3M™ Unitek™ OrthoForm™	300-027	FDA UDI	Class I	Active
3M™ Unitek™	163-366	FDA UDI	Class I	Active
APC™ II Victory Series™ Superior Fit	3069-6313	FDA UDI	Class II	Active
APC™ II Unitek™ Gemini	3027-308	FDA UDI	Class II	Active
3M™ Unitek™	163-361	FDA UDI	Class I	Active
3M™ Unitek™	160-376	FDA UDI	Class I	Active
3M™ Victory Series™	905-115	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-898	FDA UDI	Class II	Active
3M™ Unitek™	141-302	FDA UDI	Class I	Active
3M™ Victory Series™	953-483	FDA UDI	Class I	Active
3M™ Unitek™	9293-935	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	024-604	FDA UDI	Class I	Active
APC™ II Clarity™ ADVANCED	3006-262	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-104	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	068-947	FDA UDI	Class I	Active
3M™ Victory Series™	905-257	FDA UDI	Class I	Active
APC™ PLUS Clarity™ SL	5007-133	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	068-945	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-779	FDA UDI	Class II	Active
APC™ PLUS Unitek™ Mini Uni-Twin	5020-965	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-653	FDA UDI	Class II	Active
APC™ PLUS Unitek™ Mini Uni-Twin	5020-466	FDA UDI	Class II	Active
3M™ Unitek™	4296-181	FDA UDI	Class I	Active
APC™ PLUS SmartClip™ SL3	5004-329	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-684	FDA UDI	Class II	Active
APC™ II SmartClip™ SL3	3004-507	FDA UDI	Class II	Active
3M™ Unitek™	295-111	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

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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.