Pointnix Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pointnix Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Last cleared in 2023. Active since 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pointnix Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gms Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Pointnix Co., Ltd.
2 devices