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Aortic Disease Articles & Analysis: Older

16 news found

News - Zero Contrast EVAR Round Table

News - Zero Contrast EVAR Round Table

In this round table discussion, 5 European experts present current evidence and their experience about the use of CO2 in the treatment of aortic diseases . Moreover, the panellists discuss all important benefits and drawbacks of the technique and present for the first time the study protocol of the prospective CO2 EVAR ...

ByAngiodroid Spa


Terumo Aortic Announces US FDA Approval for Thoraflex Hybrid

Terumo Aortic Announces US FDA Approval for Thoraflex Hybrid

Terumo Aortic today announced that the US Food and Drug Administration (FDA) has granted approval of the Thoraflex Hybrid Frozen Elephant Trunk (FET) device for commercial sale in the United States for the treatment of patients with complex aortic arch disease. ...

ByTerumo Aortic


Anteris reports successful interim results for the first-in-human trial for DurAVR

Anteris reports successful interim results for the first-in-human trial for DurAVR

JACC CV Imag. 2019;12(1):25-34) Mack et al. Transcatheter Aortic-Valve Replacement with a Balloon-Expandable Valve in Low-Risk Patients/Supplementary Appendix N Engl J Med 2019; 380:1695-1705 Gorlin et al. Dynamics of the circulation in aortic valvular disease., Am J Med. 1955 Jun;18(6):855-70 About Anteris Technologies Ltd (ASX: AVR) ...

ByAnteris Technologies Limited


JenaValve Announces Strategic Investment and Licensing Agreement with Peijia Medical Limited

JenaValve Announces Strategic Investment and Licensing Agreement with Peijia Medical Limited

” “With the addition of the TrilogyTM, Peijia will have a more comprehensive product portfolio to better serve patients with aortic valve diseases in China,” said Dr. Yi Zhang, Peijia’s Chairman, and Chief Executive Officer. ...

ByJenaValve Technology, Inc.


JenaValve Announces First European Commercial Implants with the Trilogy™ Heart Valve System

JenaValve Announces First European Commercial Implants with the Trilogy™ Heart Valve System

The procedures, which included treatment of both aortic regurgitation1 (AR) and aortic stenosis1 (AS), took place in multiple centers in Germany, marks the official start of the European commercial launch of Trilogy. The Trilogy Heart Valve System is the first and only transfemoral TAVR system in the world indicated for the treatment of aortic ...

ByJenaValve Technology, Inc.


IOPS Symposium at VAM 2021

IOPS Symposium at VAM 2021

Several challenging IOPS cases were presented as well as dialogue with an audience of distinguished vascular surgeons treating complex aortic ...

ByCenterline Biomedical


JenaValve Receives IDE Approval to Initiate The ALIGN-AR Pivotal PMA Trial

JenaValve Receives IDE Approval to Initiate The ALIGN-AR Pivotal PMA Trial

JenaValve Technology, Inc., developer, and manufacturer of differentiated transcatheter aortic valve replacement (TAVR) systems, today announced FDA approval for the company to initiate its Investigational Device Exemption (IDE) PMA clinical trial for the Trilogy™ Heart Valve System for severe symptomatic, high-surgical risk aortic regurgitation. ...

ByJenaValve Technology, Inc.


JenaValve Technology Receives CE Mark for its Trilogy TAVI System for the Treatment of Aortic Regurgitation and Aortic Stenosis

JenaValve Technology Receives CE Mark for its Trilogy TAVI System for the Treatment of Aortic Regurgitation and Aortic Stenosis

JenaValve Technology, Inc., developer, and manufacturer of differentiated transcatheter aortic valve implantation (TAVI) systems (also referred to as TAVR, or transcatheter aortic valve replacement) for the treatment of aortic valve disease, today announced that it has received CE Mark for its TrilogyTM Heart Valve System for the ...

ByJenaValve Technology, Inc.


JenaValve Technology Welcomes Jane Metcalf as Vice President, Regulatory Affairs and Quality

JenaValve Technology Welcomes Jane Metcalf as Vice President, Regulatory Affairs and Quality

JenaValve Technology, Inc., developer and manufacturer of differentiated pericardial transcatheter aortic valve replacement (TAVR) systems for the treatment of aortic valve disease, announces the appointment of Jane Metcalf toVice President, Regulatory Affairs and Quality, effective immediately. ...

ByJenaValve Technology, Inc.


Endospan Enrolls First Patient in the TRIOMPHE IDE Study

Endospan Enrolls First Patient in the TRIOMPHE IDE Study

Endospan, a pioneer in off-the-shelf endovascular repair of aortic arch disease, announces the first implant of the NEXUS™ Aortic Arch Stent Graft System on a patient with a thoracic aortic aneurysm as part of the TRIOMPHE Study in Norfolk, Virginia, January 11, 2021. ...

ByEndospan Ltd.


Centerline Biomedical Kicks Off First Clinical Study of Intra-Operative Positioning System Technology

Centerline Biomedical Kicks Off First Clinical Study of Intra-Operative Positioning System Technology

First clinically deployed overseas in 2019, and with many cases completed in the US in 2020, IOPS™ is used during endovascular aortic interventions and allows navigation and placement of catheters and guidewires with reduced dependence on X-ray fluoroscopy, to which it serves as an adjunct, providing high-definition 3-D color image guidance using electromagnetic tracking ...

ByCenterline Biomedical


FDA Grants NEXUS Aortic Arch Stent Graft System Breakthrough Designation

FDA Grants NEXUS Aortic Arch Stent Graft System Breakthrough Designation

Endospan, a pioneer in off-the-shelf endovascular repair of aortic arch disease was recently granted Breakthrough Device Designation from the U.S. ...

ByEndospan Ltd.


JenaValve Technology Closes $50 Million Financing

JenaValve Technology Closes $50 Million Financing

JenaValve Technology, Inc., developer and manufacturer of the JenaValve Pericardial Transcatheter Aortic Valve Replacement (TAVR) System for the treatment of aortic valve disease, announces that it has raised $50 million in an equity financing led by Bain Capital Life Sciences. ...

ByJenaValve Technology, Inc.


Endospan Enters Into Strategic Distribution Agreement With CryoLife

Endospan Enters Into Strategic Distribution Agreement With CryoLife

” Minimally invasive techniques are standard-of-care for treating descending aortic disease and heart disease, but highly invasive, high-mortality open surgery is still being used in the difficult-to-treat aortic arch anatomy. ...

ByEndospan Ltd.


Endospan elects Jeff Elkins as a director

Endospan elects Jeff Elkins as a director

Endospan, a pioneer in off-the-shelf endovascular repair of Aortic Arch Disease including aneurysms and dissections, today announced that it has elected Jeff Elkins to its board of directors. ...

ByEndospan Ltd.


Endospan receives CE mark for HORIZON EVAR system based on robust clinical and pivotal data to treat Abdominal Aortic Aneurysm (AAA)

Endospan receives CE mark for HORIZON EVAR system based on robust clinical and pivotal data to treat Abdominal Aortic Aneurysm (AAA)

Endospan, a pioneer in off-the-shelf EndoVascular Aortic Repair (EVAR), announced today that it has received CE marking for its HORIZON Stent Graft System to treat Abdominal Aortic Aneurysm (AAA). ...

ByEndospan Ltd.

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