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Cardiovalve

On December 7th, 2021, Venus Medtech announced the acquisition of Cardiovalve Ltd. The Cardiovalve system independently developed by the company is a transcatheter interventional replacement product for patients suffering from mitral or tricuspid regurgitation. Compared with products of the same kind, its transfemoral approach improves the safety of treatment in significant ways.

Cardiovalve’s treatment of mitral regurgitation has entered clinical trials in Europe and is currently in an early feasibility study in the U.S.. Furthermore, its device for the treatment of tricuspid regurgitation received 'Breakthrough Device Designation' by the FDA in January 2020 and entered an early feasibility study. It is worth mentioning that Cardiovalve is also the first privately held company to receive FDA's early feasibility study (EFS) approval for both TR and MR indications. 

For more information, please click::http://www.cardiovalve.com/

DragonFly™

The DragonFly MitraClip System ("DragonFlyTM"), independently developed by Valgen Medtech, is the first domestically engineered transfemoral mitral valve clip system approved in China. DragonFlyTM entered the NMPA's Special Review and Approval Procedures for Innovative Medical Devices in March 2021 and received marketing approval on November 29, 2023.

Venus Medtech and Valgen Medtech jointly announced that both parties reached an exclusive strategic marketing cooperation intention in relation to the DragonFly MitraClip System of Valgen Medtech on November 22nd, 2023. Both parties will carry out in-depth commercialization cooperation after the approval for listing of DragonFlyTM.Both parties will join hands and firmly believe that the cooperation will accelerate the development of the diagnosis and treatment of valvular heart diseases in China, and lay a solid foundation for building a comprehensive diagnosis and treatment platform for structural heart diseases in China in the future.