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Displaying 101 - 120 of 154
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FDA Approves Lotus Edge, Ushering Third Device Into US Market
News Daily News

FDA Approves Lotus Edge, Ushering Third Device Into US Market

Shelley Wood
Shelley Wood
April 24, 2019
News Industry News

Boston Scientific Receives FDA Approval for LOTUS Edge™ Aortic Valve System

April 23, 2019
FDA Grants Approval to TherOx for Supersaturated Oxygen Therapy in LAD STEMI
News Daily News

FDA Grants Approval to TherOx for Supersaturated Oxygen Therapy in LAD STEMI

L.A. McKeown
L.A. McKeown
April 04, 2019
FDA Extends MitraClip Indication to Include Functional MR
News Daily News

FDA Extends MitraClip Indication to Include Functional MR

Shelley Wood
Shelley Wood
March 14, 2019
FDA Approves Orsiro Ultrathin-Strut Stent for CAD
News Daily News

FDA Approves Orsiro Ultrathin-Strut Stent for CAD

Michael O'Riordan
Michael O'Riordan
February 22, 2019
TCTMD’s Top 10 Most Popular Stories for January 2019
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for January 2019

Caitlin E. Cox
Caitlin E. Cox
January 31, 2019
FDA Approves Pea-Sized Occluder for Patent Ductus Arteriosus in Premature Babies
News Daily News

FDA Approves Pea-Sized Occluder for Patent Ductus Arteriosus in Premature Babies

L.A. McKeown
L.A. McKeown
January 14, 2019
FDA Clears Next-Generation Sapien 3 Ultra TAVR Valve
News Daily News

FDA Clears Next-Generation Sapien 3 Ultra TAVR Valve

Todd Neale
Todd Neale
January 02, 2019
European Regulators Strike Secondary Prevention Claim for Omega-3 Drugs
News Daily News

European Regulators Strike Secondary Prevention Claim for Omega-3 Drugs

Shelley Wood
Shelley Wood
December 18, 2018
FDA Advisors Give Blessing to Implantable Pulse Generator in Certain Heart Failure Patients
News Daily News

FDA Advisors Give Blessing to Implantable Pulse Generator in Certain Heart Failure Patients

Yael L. Maxwell
Yael L. Maxwell
December 05, 2018
Diabetes Drug Canagliflozin Gets MACE Reduction Indication
News Daily News

Diabetes Drug Canagliflozin Gets MACE Reduction Indication

Todd Neale
Todd Neale
November 01, 2018
FDA Puts the Kibosh on Canakinumab for Cardiac Indication—at Least for Now
News Daily News

FDA Puts the Kibosh on Canakinumab for Cardiac Indication—at Least for Now

Michael O'Riordan
Michael O'Riordan
November 01, 2018
FDA Approves HeartMate 3 as Destination Therapy in Advanced HF
News Daily News

FDA Approves HeartMate 3 as Destination Therapy in Advanced HF

Michael O'Riordan
Michael O'Riordan
October 19, 2018
FDA Approves Rivaroxaban for CV Event Reduction in CAD and PAD Patients
News Daily News

FDA Approves Rivaroxaban for CV Event Reduction in CAD and PAD Patients

Todd Neale
Todd Neale
October 12, 2018
FDA Approves BioMimics 3D Stent for Femoropopliteal Artery Disease
News Daily News

FDA Approves BioMimics 3D Stent for Femoropopliteal Artery Disease

Caitlin E. Cox
Caitlin E. Cox
October 05, 2018
Eluvia Gains FDA Approval Just Days After IMPERIAL Results Released
News Conference News TCT 2018

Eluvia Gains FDA Approval Just Days After IMPERIAL Results Released

Todd Neale
Todd Neale
September 24, 2018
FDA Approves New Covered Stent Option for Coronary Perforations
News Daily News

FDA Approves New Covered Stent Option for Coronary Perforations

Todd Neale
Todd Neale
September 14, 2018
CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence
News Daily News

CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

Caitlin E. Cox
Caitlin E. Cox
September 05, 2018
‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions
News Daily News

‘The Bleeding Edge’ Documentary, Tackling Medical Device Regulation, Spurs Diverse Cardiology Reactions

Yael L. Maxwell
Yael L. Maxwell
August 17, 2018
High-Risk Medical Device Approval Process in Europe Inches Towards Transparency
News Daily News

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

Michael O'Riordan
Michael O'Riordan
July 20, 2018

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