510(k) K212680

Device
LuxCreo Clear Aligner System
Applicant
LuxCreo, Inc.
510(k) number
K212680
Product code
NXC
Decision
Substantially Equivalent (SESE)
Decision date
2022-05-31
Date received
2021-08-24
Regulation
872.5470
Classification name
Aligner, Sequential
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Mike Yang
Address
940 Old County Rd. Belmont CA US 94002 94002

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code NXC#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K251758Serafin®Tns Co., Ltd.2025-09-11
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K242637MEM Clear Aligner SystemMem Dental Technology Co., Ltd.2025-05-21
K250343LuxCreo Clear Aligner SystemLuxCreo, Inc.2025-04-08
K250487SparkTM Clear Aligner SystemOrmco Corporation2025-02-20
K242715Pearl Clear AlignerPearl Digital, Inc.2025-01-16