Invisalign Pre-Formed Attachment System

Invisalign Pre-Formed Attachment System positions patient-specific attachments for bonding to teeth during aligner treatment. The attachments assist aligner retention and the force system…

Registry build 21.09.26

Invisalign Pre-Formed Attachment System positions patient-specific attachments for bonding to teeth during aligner treatment. The attachments assist aligner retention and the force system used for tooth movement.

The preformed attachments are additively manufactured from a fully cured, photopolymerizable methacrylate-based resin. Their shapes and placement follow the patient’s approved treatment plan and tooth anatomy.

Listed Item

The Invisalign Pre-Formed Attachment System is a doctor prescribed, patient specific system for the bonding of 3D-printed attachments onto the patient’s teeth. The pre-formed attachment system contains two sets of attachment positioners for each quadrant that requires attachments.

Treatment Planning

The doctor prescribes attachments as part of the aligner plan and reviews the plan through ClinCheck software before manufacture. The attachment system supports transfer and bonding of the prescribed shapes at the required tooth locations.

14manufacturers in China registered for this device type
2catalogue numbers in this listing
12510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (4), Zhejiang (2), Jiangsu (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NXC
Manufacturer City Province Registered as Device types
Ningbo Sezen Technology Co., Ltd. Ningbo Zhejiang Contract manufacturer 7
Envista (Suzhou) Medical Device Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Envista (Sichuan) Medical Device Co., Ltd. Ziyang Sichuan Contract manufacturer 4
Sichuan Yinli Medical Equipment Co., Ltd. Ziyang Sichuan Contract manufacturer 1
Xi’an Henghui Technology, Ltd Xi’An Shaanxi Contract manufacturer 1
Aidite (Qinhuangdao) Technology Co., Ltd. Qinhuangdao Hebei Repacker / relabeller 17
Shandong Huge Dental Material Corporation Rizhao Shandong Manufacturer 17
Shenzhen Sunmc Dental Technology Co., Ltd. Shenzhen Guangdong Manufacturer 17
Modern Dental Laboratory (DG) Co., Ltd. Dongguan Guangdong Contract manufacturer 15
Royal Dental Lab Shenzhen Guangdong Manufacturer 12
Wuxi EA Medical Instruments Technologies Limited Wuxi Jiangsu Repacker / relabeller 6
Shanghai Smartee Denti-Technology Co., Ltd. Shanghai Shanghai Exporter 5

Showing 12 of 14. All 14 manufacturers in China registered for Aligner, Sequential

Record

Regulatory record for Invisalign Pre-Formed Attachment System
Listed by Align Technology, Inc., United States
FDA product code NXC
Device type Aligner, Sequential
Device class Class 2
Regulation 21 CFR 872.5470
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K222894
Record published 2023-07-24

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Invisalign Pre-Formed Attachment System
Catalogue number Size Status
9030 In distribution
5000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SLX® Clear Aligners Ortho Organizers, Inc. 176
Reveal® Aligners Ortho Organizers, Inc. 149
Reveal® Clear Aligners Ortho Organizers, Inc. 148
ClearArc Aligners Ortho Organizers, Inc. 148
Risas Reveal® Aligners Ortho Organizers, Inc. 140
Absolute® Clear Aligners Ortho Organizers, Inc. 65
3M™ Clarity™ 3M Unitek 56
Reveal™ Aligners Henry Schein, Inc. 52
Clear Image Aligner Specialty Appliances, LLC 35
Spark Ormco Corporation 16
Clarity™ Aligners 3M Unitek 14
Clarity™ Solventum Orthodontics Corporation 13

Showing 12 of 232. All products under Aligner, Sequential

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252931 2025-10-23
K252870 2025-10-09
K252380 2025-08-29
K241412 2024-06-18
K232887 2023-12-15
K232233 2023-09-26
K222894 2022-12-22
K220287 2022-04-07
K181739 2018-10-26
K143630 2015-11-18
K081960 2008-12-17
K981095 1998-09-08

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer