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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 4 of 168

Device	Model / Reference	Registries	Class	Status
3M™ AlastiK™	406-299	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-627	FDA UDI	Class II	Active
APC™ PLUS Clarity™ ADVANCED	5006-221	FDA UDI	Class II	Active
Clarity™ Aligners	70000916695	FDA UDI	Class II	Active
3M™ Unitek™	801-713	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-659	FDA UDI	Class II	Active
Clarity™ ADVANCED	006-110	FDA UDI	Class II	Unknown
3M™ Unitek™	341-321	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-797	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-6570	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5017-619	FDA UDI	Class II	Active
APC™ PLUS Victory Series™	5067-9092	FDA UDI	Class II	Active
3m™	4024-131	FDA UDI	Class II	Active
3M™ Unitek™	149-231	FDA UDI	Class I	Active
3M™ Victory Series™	957-117	FDA UDI	Class I	Active
3m™	504-201	FDA UDI	Class II	Active
3M™ AlastiK™	406-976	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™ MBT™	024-909B	FDA UDI	Class I	Active
APC™ II Clarity™ SL	3007-123	FDA UDI	Class II	Active
Clarity™ Aligners	70000916729	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™ MBT™	024-7970B	FDA UDI	Class I	Active
APC™ Flash-Free SmartClip™ SL3	4004-409	FDA UDI	Class II	Active
3M™ Unitek™	161-101	FDA UDI	Class I	Active
3M™ Unitek™	147-406	FDA UDI	Class I	Active
3M™ Unitek™	9296-517	FDA UDI	Class I	Active
3M™ Unitek™	801-707	FDA UDI	Class I	Active
APC™ II Unitek™ Gemini	3119-715	FDA UDI	Class II	Active
APC™ II Clarity™ SL	3007-439	FDA UDI	Class II	Active
APC™ PLUS Clarity™ SL	5007-125	FDA UDI	Class II	Active
3M™ Unitek™	163-480	FDA UDI	Class I	Active
3M™ Unitek™ Uni-Twin™	020-516	FDA UDI	Class I	Active
3M™ Unitek™ OrthoForm™	300-965	FDA UDI	Class I	Active
3M™ Victory Series™	953-487	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	024-608	FDA UDI	Class I	Active
3M™ Victory Series™	902-469	FDA UDI	Class I	Active
3M™ Unitek™ Uni-Twin™	020-477	FDA UDI	Class I	Active
3M™ Unitek™ OrthoForm™	293-321	FDA UDI	Class I	Active
3M™ Unitek™	9293-882	FDA UDI	Class I	Active
3M™ Unitek™ Victory Series™	069-6213	FDA UDI	Class I	Active
APC™ II Victory Series™	3017-4310	FDA UDI	Class II	Active
Clarity™ SL APC™ II SmartClip™ SL3	3007-131	FDA UDI	Class II	Active
3M™ Unitek™	390-120	FDA UDI	Class I	Active
APC™ Flash-Free Victory Series™ Low Profile	4024-508	FDA UDI	Class II	Active
3M™ Unitek™	9293-891	FDA UDI	Class I	Active
APC™ II Victory Series™ V-Slot	3017-933	FDA UDI	Class II	Active
3M™ Unitek™ Victory Series™	024-510	FDA UDI	Class I	Active
APC™ PLUS Victory Series™	5017-678	FDA UDI	Class II	Active
APC™ II Victory Series™ Superior Fit	3069-6213	FDA UDI	Class II	Active
APC™ Flash-Free SmartClip™ SL3	4004-435	FDA UDI	Class II	Active
APC™ II Victory Series™	3017-895	FDA UDI	Class II	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.