SILVER SPRING, Md., June 3, 2021 /PRNewswire/ -- The U.S. Food and Drug Administration is alerting health care providers to no longer implant end-stage heart failure patients with Medtronic's ...

ST. PAUL, Minn.-- (BUSINESS WIRE)--St. Jude Medical, Inc. (NYSE:STJ), a global medical device company, today announced the company has received an Innovation Award for its HeartMate 3 ™ Left ...

Approximately one year after the company landed FDA approval for its Ventricular Assist System, the company is boasting significant surge in revenue. In early morning trading on November 7, the ...

Fresh off a Class I recall, HeartWare International ($HTWR) revealed more safety woes Thursday. The company issued a voluntary correction notice about earlier-than ...

PLEASANTON, Calif. -- Thoratec Corporation, a world leader in device-based mechanical circulatory support therapies to save, support and restore failing hearts, said today it has acquired the ...

As the med tech industry casts its eye toward next-generation devices for severe cardiac conditions, physicians are weighing in on the products' efficacy in treating patients with heart failure.

HeartWare's ENDURANCE clinical trial is a prospective, randomized, controlled, un-blinded Investigational Device Exemption (IDE) study designed to evaluate the HeartWare ® Ventricular Assist System as ...

FRAMINGHAM, Mass. and SYDNEY, Jan. 9, 2012 /PRNewswire/ -- HeartWare International, Inc. (NASDAQ: HTWR - ASX: HIN), a leading innovator of less invasive, miniaturized circulatory support technologies ...

LONDON--(BUSINESS WIRE)--Technavio has been monitoring the global ventricular assist devices market since 2015 and the market is poised to grow by USD 943.27 million during 2020-2024 at a CAGR of ...

Tong, Z. , Gou, Z. and Tan, J. (2025) A PID-Based Speed Modulation Method for Left Ventricular Assist Devices. Open Journal of Applied Sciences, 15, 3780-3794. doi: 10.4236/ojapps.2025.1511245 .

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. The FDA has designated Medtronic’s recall of two parts ...

An “Urgent Medical Device Correction” issued by Abbott-Thoratec for its HeartMate II LVAS Pocket System Controller has been classified by the US Food and Drug Administration (FDA) as a class I recall, ...