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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 5 of 168

Device	Model / Reference	Registries	Class	Status
APC™ PLUS Victory Series™	5017-413	FDA UDI	Class II	Active
3M™ Unitek™	801-721	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-504	FDA UDI	Class II	Active
APC™ II Unitek™ Miniature Twin V-Slot	3017-389	FDA UDI	Class II	Active
APC™ PLUS SmartClip™ SL3	5004-2420	FDA UDI	Class II	Active
3M™ Unitek™ OrthoForm™	300-906	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-7160	FDA UDI	Class II	Active
APC™ Flash-Free SmartClip™ SL3	4004-2480	FDA UDI	Class II	Active
3M™ Unitek™	160-271	FDA UDI	Class I	Active
3M™ Unitek™	149-201	FDA UDI	Class I	Active
3M™ Unitek™ Uni-Twin™	020-415	FDA UDI	Class I	Active
APC™ II Victory Series™ Superior Fit	3069-5163	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-517	FDA UDI	Class II	Active
APC™ II Clarity™ SL	3007-549	FDA UDI	Class II	Active
APC™ PLUS Clarity™ SL	5007-120	FDA UDI	Class II	Active
3M™ Victory Series™	957-217	FDA UDI	Class I	Active
3M™ Victory Series™	953-271	FDA UDI	Class I	Active
3M™ Victory Series™	952-162	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-100	FDA UDI	Class II	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-8950	FDA UDI	Class II	Active
3M™ Unitek™ Uni-Twin™	020-175	FDA UDI	Class I	Active
APC™ PLUS Clarity™ SL	5007-523	FDA UDI	Class II	Active
3M™ Clarity™	358-505	FDA UDI	Class II	Active
3M™ Wax-Pak™	603-063	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-622	FDA UDI	Class II	Active
3M™ Unitek™	119-172	FDA UDI	Class I	Active
3M™ Unitek™	4582-302	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-7010	FDA UDI	Class II	Active
3M™ Victory Series™	902-471	FDA UDI	Class I	Active
APC™ Flash-Free SmartClip™ SL3	4004-414	FDA UDI	Class II	Active
3M™ Unitek™	145-212	FDA UDI	Class I	Active
Unitek™ Gemini Clear	117-103	FDA UDI	Class II	Active
APC™ PLUS Victory Series™ V-Slot	5017-920	FDA UDI	Class II	Active
APC™ II Victory Series™ Low Profile	3024-3811	FDA UDI	Class II	Active
APC™ II Unitek™ Miniature Twin	3017-209	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	024-873B	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-757	FDA UDI	Class II	Active
APC™ II Victory Series™	3067-8791	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-580	FDA UDI	Class II	Active
APC™ II Unitek™ Miniature Twin	3017-378	FDA UDI	Class II	Active
3M™ Unitek™	141-199	FDA UDI	Class I	Active
3M™ AlastiK™	406-947	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5067-81938	FDA UDI	Class II	Active
3M™ Victory Series™	957-162	FDA UDI	Class I	Active
3M™ Victory Series™	952-382	FDA UDI	Class I	Active
APC™ II Unitek™ Mini Uni-Twin	3020-9540	FDA UDI	Class II	Active
3M™ Unitek™	149-214	FDA UDI	Class I	Active
3M™ Victory Series™	955-116	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-809	FDA UDI	Class II	Active
3M™ Victory Series™	953-275	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.