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Pi-Cardia Successfully Completes First-in-Human Studies with Novel Non-implant Based Treatment of Aortic Stenosis

May 07, 2019

News Industry News

Essential Medical Announces Positive Results from The Safe Manta Clinical Trial, The First Pivotal Trial for a Dedicated Large Bore Closure Device

June 25, 2018

News Industry News

Essential Medical Inc. Announces CE Mark Approval for the MANTA™ Large Bore Vascular Closure Device

July 18, 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

Essential Medical Inc. Announces Successful Completion of EU Clinical Studies for MANTA™ Large Bore Vascular Closure Device

January 31, 2016

News Industry News

Essential Medical Inc. Announces Successful Commencement of EU Studies for MANTA™ Large Bore Vascular Closure Device

July 27, 2015

News Industry News

Essential Medical Inc. Announces Successful Additional Clinical Studies For MANTA™ Large Bore Vascular Closure Device

May 04, 2015

News Industry News

Covidien Neurovascular Micro Catheter Receives FDA Approval

June 10, 2014

News Industry News

Medtronic Expands Availability of Market-Leading Aortic & Peripheral Solutions to U.S. Market

June 04, 2014

News Industry News

Valiant Captivia Thoracic Stent Graft System From Medtronic Receives FDA Approval for Treating Aortic Dissections

January 27, 2014

News Industry News

Intervalve Inc. Receives 510(k) Clearance in the United States for the V8 Aortic Valvuloplasty Balloon Catheter

April 26, 2013

News Industry News

Loma Vista Medical reports that it is ramping up sales in U.S. and Europe of its FDA-cleared and CE-marked TRUE Dilatation™ Balloon Valvuloplasty Catheter

February 12, 2013

News Industry News

Loma Vista Medical receives FDA clearance for its TRUE Dilatation™ Balloon Valvuloplasty Catheter

October 17, 2012

News Industry News

Loma Vista Medical receives CE mark for its TRUE Dilatation™ Balloon Valvuloplasty Catheter

May 10, 2012

News Industry News

PARTNER QoL data hint transapical TAVI falls short of aortic-valve surgery

November 09, 2011

News Industry News

First Research Results of Angiomax(R) (Bivalirudin) Versus Heparin in Transcatheter Aortic Valve Interventions Reported at TCT

November 07, 2011

News Industry News

St. Jude Medical Announces FDA Approval of Trifecta Valve

April 20, 2011

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Pi-Cardia Successfully Completes First-in-Human Studies with Novel Non-implant Based Treatment of Aortic Stenosis

Essential Medical Announces Positive Results from The Safe Manta Clinical Trial, The First Pivotal Trial for a Dedicated Large Bore Closure Device

Essential Medical Inc. Announces CE Mark Approval for the MANTA™ Large Bore Vascular Closure Device

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

Essential Medical Inc. Announces Successful Completion of EU Clinical Studies for MANTA™ Large Bore Vascular Closure Device

Essential Medical Inc. Announces Successful Commencement of EU Studies for MANTA™ Large Bore Vascular Closure Device

Essential Medical Inc. Announces Successful Additional Clinical Studies For MANTA™ Large Bore Vascular Closure Device

Covidien Neurovascular Micro Catheter Receives FDA Approval

Medtronic Expands Availability of Market-Leading Aortic & Peripheral Solutions to U.S. Market

Valiant Captivia Thoracic Stent Graft System From Medtronic Receives FDA Approval for Treating Aortic Dissections

Intervalve Inc. Receives 510(k) Clearance in the United States for the V8 Aortic Valvuloplasty Balloon Catheter

Loma Vista Medical reports that it is ramping up sales in U.S. and Europe of its FDA-cleared and CE-marked TRUE Dilatation™ Balloon Valvuloplasty Catheter

Loma Vista Medical receives FDA clearance for its TRUE Dilatation™ Balloon Valvuloplasty Catheter

Loma Vista Medical receives CE mark for its TRUE Dilatation™ Balloon Valvuloplasty Catheter

PARTNER QoL data hint transapical TAVI falls short of aortic-valve surgery

First Research Results of Angiomax(R) (Bivalirudin) Versus Heparin in Transcatheter Aortic Valve Interventions Reported at TCT

St. Jude Medical Announces FDA Approval of Trifecta Valve

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