LuxCreo, Inc. - FDA 510(k) Cleared Devices
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..
4 devices