Edwards Lifesciences welcomes CMS TAVR coverage update
The company reaffirms its 2026 financial guidance and highlights improved patient access for transcatheter aortic valve replacement procedures.
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Structural heart medical device manufacturer
edwards.comLast updated
In short: Edwards won FDA approvals, delivered strong quarterly results, raised guidance, and faced regulatory penalties.
The company reaffirms its 2026 financial guidance and highlights improved patient access for transcatheter aortic valve replacement procedures.
Second quarter sales grew 13.6% to $1.74 billion, driven by TAVR and structural heart therapies. The company increases its full-year constant currency sales growth forecast to 10-11%. Updated financial projections confirm adjusted EPS guidance of $2.95 to $3.05.
The company recorded $1.7 billion in sales and recognized significant impairment losses totaling $163.6 million.
Sales rose to $1.74B, driven by TAVR and TMTT; adjusted EPS of $0.78 beat expectations.
The FDA's approval in tricuspid regurgitation adds the clip-based Pascal Precision alongside Edwards' Evoque implant for replacing the valve.
Edwards said FDA approval of Pascal Ace with capture clarity simplifies mitral TEER procedures for clinicians. Edwards Lifesciences reported that FDA has approved its Pascal...
The US FDA on Thursday warned of a potentially high-risk issue involving certain Edwards Lifescien...
Edwards Lifesciences reported double-digit fourth-quarter sales growth and said expanding demand for its · structural heart therapies is strengthening the company’s confidence in continued growth...
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