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News Daily News

Volt Pulsed-Field Ablation System Gains FDA Approval

Todd Neale

December 24, 2025

News Daily News

FDA Approves Sapien M3 for Transseptal Mitral Valve Replacement

Michael O'Riordan

December 23, 2025

News Daily News

FDA Approves Cordella Remote PA Pressure Monitoring System for HF

Yael L. Maxwell

June 24, 2024

News Daily News

FDA Approves Bioresorbable Scaffold for BTK Lesions

Michael O'Riordan

April 29, 2024

News Daily News

FDA Approves TriClip TEER Device for Tricuspid Repair

L.A. McKeown

April 02, 2024

News Daily News

FDA Approves First Transcatheter Tricuspid Valve Replacement Device

L.A. McKeown

February 02, 2024

News Daily News

Top Endovascular News of 2023

L.A. McKeown

December 28, 2023

News Daily News

Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval

L.A. McKeown

July 06, 2023

News Conference News TVT 2022

Non-COAPT-Like Patients Fare Well With MitraClip, EXPAND Suggests

Michael O'Riordan

June 09, 2022

News Daily News

FDA Grants Expanded Indication to CardioMEMS PA Pressure Monitor

Shelley Wood

February 22, 2022

News Daily News

FDA Approves Portico TAVI Valve, Paving the Way for Third US Device

Shelley Wood

September 20, 2021

News Daily News

Xience Cleared in Europe for 1-Month DAPT in High-Bleeding-Risk Patients

Shelley Wood

April 06, 2021

News Daily News

European Regulators Approve First Transcatheter MV Replacement Device

Michael O'Riordan

January 30, 2020

News Daily News

FDA Extends MitraClip Indication to Include Functional MR

Shelley Wood

March 14, 2019

News Daily News

FDA Approves Orsiro Ultrathin-Strut Stent for CAD

Michael O'Riordan

February 22, 2019

News Daily News

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

L.A. McKeown

January 14, 2019

News Daily News

FDA Approves HeartMate 3 as Destination Therapy in Advanced HF

Michael O'Riordan

October 19, 2018

News Daily News

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

Caitlin E. Cox

September 05, 2018

News Conference News ACC 2018

Bad BVS News: Analysis Points to Fast Reaction by Interventionalists to Absorb Safety Issues

Michael O'Riordan

March 11, 2018

News Daily News

FDA Grants HeartWare LVAD a Destination Therapy Indication

Todd Neale

September 28, 2017

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Volt Pulsed-Field Ablation System Gains FDA Approval

FDA Approves Sapien M3 for Transseptal Mitral Valve Replacement

FDA Approves Cordella Remote PA Pressure Monitoring System for HF

FDA Approves Bioresorbable Scaffold for BTK Lesions

FDA Approves TriClip TEER Device for Tricuspid Repair

FDA Approves First Transcatheter Tricuspid Valve Replacement Device

Top Endovascular News of 2023

Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval

Non-COAPT-Like Patients Fare Well With MitraClip, EXPAND Suggests

FDA Grants Expanded Indication to CardioMEMS PA Pressure Monitor

FDA Approves Portico TAVI Valve, Paving the Way for Third US Device

Xience Cleared in Europe for 1-Month DAPT in High-Bleeding-Risk Patients

European Regulators Approve First Transcatheter MV Replacement Device

FDA Extends MitraClip Indication to Include Functional MR

FDA Approves Orsiro Ultrathin-Strut Stent for CAD

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

FDA Approves HeartMate 3 as Destination Therapy in Advanced HF

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

Bad BVS News: Analysis Points to Fast Reaction by Interventionalists to Absorb Safety Issues

FDA Grants HeartWare LVAD a Destination Therapy Indication

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