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Medtide (03880.HK): Subsidiary Zhongtai Biochemical's Hangzhou Facility Successfully Passes FDA Pre-License Inspection, Paving Way for Commercial API Production of Hepcludex®

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MEDTIDE 03880.HK FDA

2026-07-31

MICROPORT NEURO(02172.HK): NUMEN™ Helia Coil Obtains FDA Marketing Approval

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MICROPORT NEURO 02172.HK FDA

2026-05-25

PEIJIA-B(09996.HK): First Patient Implant Completed in US Early Feasibility Study of GeminiOne® TEER System

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PEIJIA-B 09996.HK FDA

2026-04-09

MICROPORT NEURO (02172.HK): APOLLO Dream® Stent System Granted FDA Breakthrough Device Designation – World’s First Neurointerventional Drug-Eluting Stent to Receive Such Designation

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MICROPORT NEURO 02172.HK FDA Breakthrough Device Designation

2026-03-18

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