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Cardiawave SA: Cardiawave Confirms the Safety of VALVOSOFT its Non-Invasive Ultrasound Treatment for Aortic Stenosis

No cerebral vascular anomaly before and after treatment observed - Successful completion of the FIM II clinical study prior to the pivotal study, that will pave the way for CE marking Cardiawave SA

Cardiawave announces French National Agency for the Safety of Medicines and Health Products (ANSM) green light to launch VALVOSOFT Pivotal Study in France

Cardiawave SA, a deeptech medical device manufacturer that has developed VALVOSOFT a revolutionary non-invasive medical device to treat aortic stenosis, the most prevalent heart valve disease in adults

Cardiawave SA: Cardiawave Announces the Success of Its Clinical Trial to Treat Aortic Stenosis Using VALVOSOFT, Its Disruptive, Non-Invasive, Ultrasound Treatment

FineHeart S A: Severe Heart Failure Treatment: FineHeart Successfully Raises €15 million Series B funding With Industrial and Independent Investors

The First In Human implantation of the ICOMS FLOWMAKER is assured following this financing FineHeart S.A, a preclinical medical device company that has developed theICOMS FLOWMAKER, an Implantable

FineHeart S A: FineHeart Breaks New Ground With Successful Removal of the ICOMS FLOWMAKER in a 90-day In-vivo Trial

FineHeart S.A: FineHeart Breaks New Ground With Successful Removal of the ICOMS FLOWMAKER in a 90-day In-vivo Trial Easy removal with a beating heart without damage to the myocardium 30 days after implantation Normal heart functioning 60 days after explantation Completely sealed operation with dedicated implant fixation system Quick recovery and short hospital stay Autonomy and free from complications or infection, or structural damage to the heart and vital organs FineHeart S.A a preclinical medical device company that has developed the ICOMS FLOWMAKER, an Implantable Cardiac Output Management System designed to address the unmet need of patients suffering from severe heart failure, today announced the successful, simple, and breakthrough implantation and removal of its device in a 90-day in-vivo trial.

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