LuxCreo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
LuxCreo, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LuxCreo Flexible Partial Denture Resin, LuxCreo Clear Aligner System, LuxCreo Dental Night Guard Resin
4
Total
4
Cleared
0
Denied
LuxCreo, Inc. has 4 FDA 510(k) cleared medical devices. Based in Belmont, US.
Latest FDA clearance: Nov 2025. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by LuxCreo, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Ruscert Technology Co., Ltd. and Shenzhen Reanny Medical Devices Management Consulting Co., Ltd..
FDA 510(k) Regulatory Record - LuxCreo, Inc.
4 devices