TCTMD

Medtronic Begins Global Clinical Study of Investigational Pericardial Surgical Aortic Heart Valve

MINNEAPOLIS- Medtronic, Inc. today announced it has initiated the PERIGON Pivotal Trial, a global, prospective clinical trial evaluating an investigational surgical aortic heart valve made from bovine ...
Business Wire

JenaValve Transcatheter Aortic Valve Replacement (TAVR) System Designated by FDA as Breakthrough Device

IRVINE, Calif.--(BUSINESS WIRE)--JenaValve Technology, Inc., developer and manufacturer of the JenaValve Pericardial transcatheter aortic valve replacement (TAVR) system for the treatment of aortic ...
Business Wire

JenaValve Technology Closes $50 Million Financing

IRVINE, Calif.--(BUSINESS WIRE)--JenaValve Technology, Inc., developer and manufacturer of the JenaValve Pericardial Transcatheter Aortic Valve Replacement (TAVR) System for the treatment of aortic ...
MassDevice

Corcym reports first U.S. implantation of next-gen sutureless aortic valve

The Lancelot technology delivers enhanced hemodynamics through the integration of precision laser cutting and after ...
TCTMD

New Data on Edwards PERIMOUNT Valves Demonstrate Long-Term Durability in Patients Aged 60 and Younger

MARSEILLE, FRANCE -- Edwards Lifesciences Corporation, the global leader in the science of heart valves and hemodynamic monitoring, today announced unprecedented long-term durability results for ...
MD&M East

Does JenaValve’s New Designation Signal the Start of Another Strong Year for TAVR?

JenaValve is showing significant progress in the plan to get its transcatheter aortic valve replacement (TAVR) system approved. FDA granted the Irvine, CA-based company Breakthrough Device Designation ...
EurekAlert!

Transcatheter aortic valve replacement -- a new frontier in cardiovascular medicine

Current experiences with one of the two CE Marked devices, the CoreValve ReValving® System for Percutaneous Aortic Valve Replacement (PAVR) have proved to be an overall success. This device consists ...
Nasdaq

EDWARDS MITRIS RESILIA VALVE RECEIVES FDA APPROVAL FOR MITRAL REPLACEMENT SURGERIES

IRVINE, Calif., March 31, 2022 /PRNewswire/ -- Edwards Lifesciences (NYSE: EW) today announced it received approval from the U.S. Food and Drug Administration (FDA) for the MITRIS RESILIA valve, a ...

FIRST U.S. IMPLANTATION OF NEXT-GENERATION PERCEVAL PLUS(R) LANCELOT VALVE

A patient in the United States has become the first in the country to receive Corcym's next-generation Perceval Plus(R) LANCELOT sutureless aortic valve, marking an important milestone in the ...
Healio

FDA approves bovine tissue valve for surgical mitral valve replacement

Please provide your email address to receive an email when new articles are posted on . Edwards Lifesciences announced the FDA approved the Mitris Resilia surgical valve, a tissue valve replacement ...
Medscape

FDA Warns of Potential Problems With Abbott Trifecta Valves

There is a potential risk of early structural valve deterioration with the Abbott Trifecta valve and Trifecta valve with glide technology (Trifecta GT), the US Food and Drug Administration (FDA) says ...