Datasea registers, lists NeuroVibe biofeedback system with FDA as Class II 510(k)-exempt device

• Datasea’s China VIE, Shuhai Jingwei, completed FDA establishment registration and device listing for its NeuroVibe Biofeedback System NV-02 and NV-03.
• Devices listed under product code HCC as Class II 510(k)-exempt biofeedback medical devices in the neurology area.
• Registration and listing do not represent FDA clearance or approval for the devices.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Datasea Intelligent Technology Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: CN23689) on August 11, 2026, and is solely responsible for the information contained therein.