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December 26, 2019

News Daily News

EACTS Calls for Independent Left Main CAD Evidence Review, Urges ESC Input

December 20, 2019

News Daily News

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

December 17, 2019

News Daily News

VICTORIA Trial of Vericiguat for Worsening HF Meets Primary Endpoint

Todd Neale

November 20, 2019

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

November 14, 2019

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

October 28, 2019

News Daily News

FDA Warns of Potential Medical Device Shortage Due to Sterilization Woes

Yael L. Maxwell

October 25, 2019

News Daily News

Implantable Cardiac Monitor May Reduce Delays to Hospital in High-Risk ACS

October 15, 2019

News Daily News

FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

October 09, 2019

News Industry News

Angel Medical Systems Inc. Assembles World-Class Medical Advisory Board

September 20, 2019

News Daily News

TCTMD’s Top 10 Most Popular Stories for August 2019

August 30, 2019

News Daily News

FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System

August 22, 2019

News Daily News

FDA Expands TAVR Indication to Low-Risk Patients

August 16, 2019

News Features

Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics

Marcus A. Banks

August 15, 2019

News Daily News

FDA: Class I Recall for Ellipse ICD Due to Faulty Wires

August 05, 2019

News Daily News

New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure

Marcus A. Banks

July 24, 2019

News Daily News

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

July 22, 2019

News Industry News

Nanowear Announces Clinical Launch of NanoSENSE, a Heart Failure Management and Alert Diagnostic Validation Study

July 22, 2019

News Daily News

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device