MicroPort NeuroTech (Shanghai) Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
MicroPort NeuroTech (Shanghai) Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Numen™ Helia Coil Embolization System, Numen™ Coil Embolization System, Numen Coil Embolization System
4
Total
4
Cleared
0
Denied
MicroPort NeuroTech (Shanghai) Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Latest FDA clearance: May 2026. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by MicroPort NeuroTech (Shanghai) Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Biodesign Regulatory Services, LLC and MicroPort CRM USA, Inc..
FDA 510(k) Regulatory Record - MicroPort NeuroTech (Shanghai) Co., Ltd.
4 devices