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News Daily News

Study Supports Noninferiority of Dedicated Bifurcation Stent: But is That Good Enough for Adoption?

Todd Neale

July 08, 2016

News Industry News

Essential Medical Inc. Announces FDA Approval to Begin a U.S. Clinical Trial for the MANTA™ Large Bore Vascular Closure Device

July 08, 2016

News Industry News

QT Vascular Receives CE Mark Clearance For Chocolate Heart™, A Novel Drug-Coated Coronary Balloon

July 07, 2016

News Industry News

Arizona patient will receive first U.S.-approved fully dissolving heart stent

July 06, 2016

News Daily News

Now You See It: FDA Approves Absorb Bioresorbable Scaffold

Michael O'Riordan

July 05, 2016

News Daily News

Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls

Shelley Wood

July 05, 2016

News Daily News

欧盟更快速核准医疗器械导致更多的安全警告和产品召回

Shelley Wood

July 05, 2016

News Daily News

Los Dispositivos Médicos Aprobados Más Rápidamente en la UE son Objeto de Más Alertas de Seguridad y Nuevas Inspecciones

Shelley Wood

July 05, 2016

News Features

Brooding Over Brexit: Cardiologists Voice Uncertainty About Effects on Collaboration, Research Funding

Yael L. Maxwell

June 29, 2016

News Industry News

CorMatrix® CanGaroo® ECM® Envelope Receives CE Mark Approval

June 28, 2016

News Industry News

QT Vascular Receives FDA 510(k) Clearance For Chocolate XD™, A Novel PTCA Balloon

June 28, 2016

News Industry News

Lombard Medical Announces CE Mark Approval for IntelliFlex™ LP Delivery System for the Aorfix™ Abdominal Aortic Aneurysm Endovascular Stent Graft

June 21, 2016

News Daily News

Proposed Legislation Could Mandate Physician Reporting of Adverse Events With Medical Devices

Yael L. Maxwell

June 14, 2016

News Daily News

New European Device Regulations Are Coming, Could Impact Speed of Approvals

Todd Neale

May 27, 2016

News Daily News

Majority of FDA Advisors Give Green Light to Amplatzer PFO Closure Device for Stroke

Shelley Wood

May 25, 2016

News Daily News

US and European Heart Failure Guidelines Advocate Use of Two New Therapies

L.A. McKeown

May 24, 2016

News Industry News

BIOTRONIK Launches CardioMessenger Smart Portable Device For Pacemaker and ICD Patients

May 24, 2016

News Industry News

iVascular Receives CE Mark Approval for LUMINOR 18 Drug Eluting Balloon

May 19, 2016

News Industry News

iVascular completes recruitment of patients for its ANCHOR clinical trial of the sirolimus eluting stent ANGIOLITE

May 19, 2016

News Conference News EuroPCR 2016

As Technique Inches Forward, Outcomes Improve for Transcatheter Treatment of Severe Calcific Mitral Disease

Shelley Wood

May 18, 2016

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Study Supports Noninferiority of Dedicated Bifurcation Stent: But is That Good Enough for Adoption?

Essential Medical Inc. Announces FDA Approval to Begin a U.S. Clinical Trial for the MANTA™ Large Bore Vascular Closure Device

QT Vascular Receives CE Mark Clearance For Chocolate Heart™, A Novel Drug-Coated Coronary Balloon

Arizona patient will receive first U.S.-approved fully dissolving heart stent

Now You See It: FDA Approves Absorb Bioresorbable Scaffold

Medical Devices Approved More Quickly in EU Face More Safety Alerts and Recalls

欧盟更快速核准医疗器械导致更多的安全警告和产品召回

Los Dispositivos Médicos Aprobados Más Rápidamente en la UE son Objeto de Más Alertas de Seguridad y Nuevas Inspecciones

Brooding Over Brexit: Cardiologists Voice Uncertainty About Effects on Collaboration, Research Funding

CorMatrix® CanGaroo® ECM® Envelope Receives CE Mark Approval

QT Vascular Receives FDA 510(k) Clearance For Chocolate XD™, A Novel PTCA Balloon

Lombard Medical Announces CE Mark Approval for IntelliFlex™ LP Delivery System for the Aorfix™ Abdominal Aortic Aneurysm Endovascular Stent Graft

Proposed Legislation Could Mandate Physician Reporting of Adverse Events With Medical Devices

New European Device Regulations Are Coming, Could Impact Speed of Approvals

Majority of FDA Advisors Give Green Light to Amplatzer PFO Closure Device for Stroke

US and European Heart Failure Guidelines Advocate Use of Two New Therapies

BIOTRONIK Launches CardioMessenger Smart Portable Device For Pacemaker and ICD Patients

iVascular Receives CE Mark Approval for LUMINOR 18 Drug Eluting Balloon

iVascular completes recruitment of patients for its ANCHOR clinical trial of the sirolimus eluting stent ANGIOLITE

As Technique Inches Forward, Outcomes Improve for Transcatheter Treatment of Severe Calcific Mitral Disease

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