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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 7 of 168

Device	Model / Reference	Registries	Class	Status
APC™ PLUS Clarity™ ADVANCED	5006-104	FDA UDI	Class II	Active
APC™ Flash-Free SmartClip™ SL3	4004-143	FDA UDI	Class II	Active
3M™ Unitek™	160-377	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-797	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	024-912	FDA UDI	Class I	Active
APC™ PLUS Victory Series™ Low Profile	5024-619	FDA UDI	Class II	Active
APC™ II Clarity™ ADVANCED	3006-255	FDA UDI	Class II	Active
APC™ II Unitek™ Mini Uni-Twin	3020-842	FDA UDI	Class II	Active
3M™ Victory Series™	957-225	FDA UDI	Class I	Active
APC™ II Unitek™ Gemini	3119-713	FDA UDI	Class II	Active
Ortholux™ Luminous	704-460	FDA UDI	Class II	Active
3M™ Victory Series™	955-255	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™ MBT™	024-776B	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Superior Fit	4069-5213	FDA UDI	Class II	Active
APC™ PLUS Clarity™ ADVANCED	5006-117	FDA UDI	Class II	Active
3M™ Victory Series™	953-462	FDA UDI	Class I	Active
3m™	329-214	FDA UDI	Class II	Active
3M™ Unitek™	160-382	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	068-987	FDA UDI	Class I	Active
3M™ Unitek™	300-111	FDA UDI	Class I	Active
3M™ Unitek™	4297-171	FDA UDI	Class I	Active
3M™ Unitek™	020-603	FDA UDI	Class I	Active
APC™ Flash-Free SmartClip™ SL3	4004-2410	FDA UDI	Class II	Active
3M™ Unitek™	4297-852	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-805	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-501	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	067-97828B	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-6830	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-5990	FDA UDI	Class II	Active
APC™ PLUS Unitek™ Miniature Twin	5017-308	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-4330	FDA UDI	Class II	Active
3M™ Unitek™	314-226	FDA UDI	Class I	Active
3M™ Forsus™	885-147	FDA UDI	Class I	Active
3M™ Unitek™	200-084	FDA UDI	Class I	Active
APC™ II Clarity™ SL	3007-539	FDA UDI	Class II	Active
3M™ Unitek™	900-752	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-7980	FDA UDI	Class II	Active
APC™ PLUS Victory Series™ Low Profile	5024-792	FDA UDI	Class II	Active
3M™ AlastiK™	406-876	FDA UDI	Class I	Active
3M™ Victory Series™	953-485	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-883	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	068-902	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-419	FDA UDI	Class II	Active
3M™ Unitek™	145-213	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-5210	FDA UDI	Class II	Active
APC™ II Unitek™ Gemini Clear	3117-408	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-432	FDA UDI	Class II	Active
3M™ Unitek™	4296-303	FDA UDI	Class I	Active
APC™ PLUS Clarity™ SL	5007-511	FDA UDI	Class II	Active
3M™ Unitek™	805-035	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.