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Edwards Lifesciences earns FDA approval for Evoque tricuspid valve

Edwards Lifesciences earns FDA approval for Evoque tricuspid valve

Edwards Lifesciences announced the company’s Evoque tricuspid valve replacement system is the first transcatheter therapy to receive FDA approval for the treatment of tricuspid regurgitation, or TR. The Evoque system is indicated for the improvement of health status in patients with symptomatic severe TR despite optimal medical therapy, or OMT, for whom tricuspid valve replacement is deemed appropriate by a heart team.

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