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Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

May 12, 2014

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St. Jude Medical Announces TOCCASTAR Clinical Trial Meets Primary Safety and Efficacy Endpoints at Heart Rhythm 2014

May 07, 2014

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EDWARDS INTUITY Valve Data Demonstrate Improved Patient Benefits Over Standard Surgical Valves

April 30, 2014

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EDWARDS INTUITY Elite Valve System Receives CE Mark

April 04, 2014

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Boston Scientific Initiates the RESPOND Post Market Registry Evaluating Clinical Outcomes in Patients Implanted With Lotus™ Valve System

June 04, 2014

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FDA Approves Expansion of BIOTRONIK ProMRI® ICD Trial to Include Full-Body Scans and DX Technology

May 22, 2014

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US FDA approves EPANOVA for the treatment of adults with severe hypertriglyceridaemia

May 06, 2014

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InspireMD Announces Voluntary Field Action for MGuard™ Prime EPS

April 30, 2014

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Boston Scientific Receives CE Mark Approval for REBEL™ Platinum Chromium Coronary Stent System

March 12, 2014

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CardioKinetix Releases One-Year Clinical Data Showing Consistent, Compelling Positive Results for Patients Treated with Minimally Invasive Structural Heart Device for Heart Failure

April 07, 2014

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Maquet Recalls Intra-Aortic Balloon Pumps Due to Potential Failure of Power Supply

St. Jude Medical Announces TOCCASTAR Clinical Trial Meets Primary Safety and Efficacy Endpoints at Heart Rhythm 2014

EDWARDS INTUITY Valve Data Demonstrate Improved Patient Benefits Over Standard Surgical Valves

EDWARDS INTUITY Elite Valve System Receives CE Mark

Boston Scientific Initiates the RESPOND Post Market Registry Evaluating Clinical Outcomes in Patients Implanted With Lotus™ Valve System

FDA Approves Expansion of BIOTRONIK ProMRI® ICD Trial to Include Full-Body Scans and DX Technology

US FDA approves EPANOVA for the treatment of adults with severe hypertriglyceridaemia

InspireMD Announces Voluntary Field Action for MGuard™ Prime EPS

Boston Scientific Receives CE Mark Approval for REBEL™ Platinum Chromium Coronary Stent System

CardioKinetix Releases One-Year Clinical Data Showing Consistent, Compelling Positive Results for Patients Treated with Minimally Invasive Structural Heart Device for Heart Failure

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