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Edwards INSPIRIS RESILIA Valve Receives CE Mark

September 29, 2016

News Industry News

Edwards Sapien 3 Transcatheter Heart Valve Receives Expanded Indication In Europe

September 19, 2016

News Industry News

EDWARDS INTUITY Elite Rapid Deployment Valve Receives FDA Approval

August 15, 2016

News Industry News

Edwards Receives Approval For SAPIEN 3 Heart Valve In Canada

July 28, 2016

News Industry News

Edwards SAPIEN 3 Transcatheter Valve Demonstrates Positive Patient Outcomes At 30 Days In European Real-World Experience

May 17, 2016

News Industry News

Corvia Medical Announces CE Mark Approval and Enrollment of First Patients in Randomized Clinical Study

May 12, 2016

News Industry News

First Patients in Central Pennsylvania Received New Aortic Valve Reconstruction Procedures at PinnacleHealth

May 03, 2016

News Industry News

HeartStitch® Launches German Sales of NobleStitch™ EL

May 02, 2016

News Industry News

Tips for Convincing Your Boss to Attend TCT 2016

April 13, 2016

News Industry News

LivaNova PLC Announces the First Patient Enrolled in the PERSIST-AVR Trial

April 04, 2016

News Industry News

First Patients Enrolled in Medtronic Trial in Low-Risk Aortic Stenosis Patients

April 01, 2016

News Industry News

Edwards Lifesciences Receives Approval For SAPIEN 3 Valve In Japan

March 16, 2016

News Industry News

Successful Transapical Access and Closure Clinical Test Performed in 6 Consecutive Invivo Procedures Using the Heartstitch TA

March 09, 2016

News Industry News

Medtronic Enrolls First Patients in Clinical Study to Evaluate the CoreValve(TM) Evolut(TM) R System in 'Real-World' Setting

March 06, 2016

News Industry News

Edwards SAPIEN XT Valve Receives FDA Approval For Pulmonic Procedures

March 01, 2016

News Industry News

Top Swedish Heart Center Confirms PFO-Closure Benefits of NobleStitch™ EL Among Widening Patient Population

February 02, 2016

News Industry News

Edwards Receives FDA Approval For Expanded Indication Study Of SAPIEN 3 Valve

January 14, 2016

News Industry News

FDA approves wearable defibrillator for children at risk for sudden cardiac arrest

December 17, 2015

News Industry News

First Patients Enrolled in the Gore RELINE MAX Clinical Study

December 15, 2015

News Industry News

Mitralign Announces Enrollment of First U.S. Subject in Percutaneous Tricuspid Repair Study

December 02, 2015

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Edwards INSPIRIS RESILIA Valve Receives CE Mark

Edwards Sapien 3 Transcatheter Heart Valve Receives Expanded Indication In Europe

EDWARDS INTUITY Elite Rapid Deployment Valve Receives FDA Approval

Edwards Receives Approval For SAPIEN 3 Heart Valve In Canada

Edwards SAPIEN 3 Transcatheter Valve Demonstrates Positive Patient Outcomes At 30 Days In European Real-World Experience

Corvia Medical Announces CE Mark Approval and Enrollment of First Patients in Randomized Clinical Study

First Patients in Central Pennsylvania Received New Aortic Valve Reconstruction Procedures at PinnacleHealth

HeartStitch® Launches German Sales of NobleStitch™ EL

Tips for Convincing Your Boss to Attend TCT 2016

LivaNova PLC Announces the First Patient Enrolled in the PERSIST-AVR Trial

First Patients Enrolled in Medtronic Trial in Low-Risk Aortic Stenosis Patients

Edwards Lifesciences Receives Approval For SAPIEN 3 Valve In Japan

Successful Transapical Access and Closure Clinical Test Performed in 6 Consecutive Invivo Procedures Using the Heartstitch TA

Medtronic Enrolls First Patients in Clinical Study to Evaluate the CoreValve(TM) Evolut(TM) R System in 'Real-World' Setting

Edwards SAPIEN XT Valve Receives FDA Approval For Pulmonic Procedures

Top Swedish Heart Center Confirms PFO-Closure Benefits of NobleStitch™ EL Among Widening Patient Population

Edwards Receives FDA Approval For Expanded Indication Study Of SAPIEN 3 Valve

FDA approves wearable defibrillator for children at risk for sudden cardiac arrest

First Patients Enrolled in the Gore RELINE MAX Clinical Study

Mitralign Announces Enrollment of First U.S. Subject in Percutaneous Tricuspid Repair Study

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