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May 01, 2025

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Little Pre- and Postmarket Testing for Most Recalled CV Devices

September 16, 2024

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FDA Approves Bioresorbable Scaffold for BTK Lesions

April 29, 2024

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Biologic Winrevair Wins FDA Approval for Treatment of PAH

March 27, 2024

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Mechanism’s Mojo: ‘Obvious’ CV Therapies More Likely to Be Seen as Effective

February 23, 2024

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FDA Approves Blood Flow-Diverting LimFlow System for No-Option CLTI

September 12, 2023

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Aveir DR Dual-Chamber Leadless Pacemaker Wins FDA Approval

July 06, 2023

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Medical Devices Cleared on Faulty Predicates More Likely to be Recalled

January 17, 2023

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Higher Annual TAVI Volumes Linked to Greater Use of Embolic Protection

August 23, 2022

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Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

June 17, 2021

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Add-on CMS Payment Sweetens Shockwave Choice, but Cost Still Rankles

May 12, 2021

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

April 06, 2021

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FDA Advisors Unconvinced by Lutonix BTK Drug-Coated Balloon

February 18, 2021

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Cryoballoon Gets FDA Approval for Persistent A-fib

Todd Neale

June 29, 2020

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FDA Extends Ticagrelor Indication to High-Risk CAD Primary Prevention

June 01, 2020

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FDA Grants Cardiac MR Indication for Gadavist Contrast Injection

July 16, 2019

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FDA Approves Lotus Edge, Ushering Third Device Into US Market

April 24, 2019

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

April 04, 2019

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FDA Extends MitraClip Indication to Include Functional MR

March 14, 2019

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