Edwards Lifesciences Corp (EW.N)
23 Aug 2016
The U.S. Food and Drug Administration has widened the use of Edwards Lifesciences Corp's heart valves to patients at intermediate risk of complications if they underwent open heart surgery.
Aug 18 The U.S. Food and Drug Administration has widened the use of Edwards Lifesciences Corp's heart valves to patients at intermediate risk of complications if they underwent open heart surgery.
* Edwards INTUITY Elite Rapid Deployment Valve receives FDA approval Source text for Eikon: Further company coverage:
* Stantec signs letter of intent to acquire NYC-based Edwards & Zuck: 120-person premiere buildings engineering firm Source text for Eikon: Further company coverage:
* Edwards Lifesciences receives approval for sapien 3 heart valve in canada Source text for Eikon: Further company coverage: (Bengaluru Newsroom +91 80 6749-1130; within U.S. +1 646 223 8780)
July 26 Edwards Lifesciences Corp on Tuesday raised its full-year earnings forecast as quarterly profits beat estimates, and said U.S. regulators would soon likely approve its minimally invasive replacement heart valve for a broader range of patients.
* Sees Q3 Sales Between $720 Mln - $760 Mln; Sees Q3 Adjusted Earnings Per Share Between $0.62 - $0.68
July 26 Edwards Lifesciences Corp on Tuesday boosted its full-year earnings outlook after posting a stronger-than-expected quarterly profit and said it expects to soon gain U.S. approval to offer its minimally invasive replacement heart valve to a broader range of patients.
April 26 Edwards Lifesciences Corp on Tuesday raised its full-year sales and profit outlook following strong first-quarter results and said approval for expanded use of its minimally invasive heart valve implant could come sooner than previously expected.
April 26 EDWARDS LIFESCIENCES CEO SAYS PLANNING FOR FDA APPROVAL, LAUNCH OF TAVR FOR INTERMEDIATE-RISK PATIENTS AT BEGINNING OF Q4 EDWARDS CEO SAYS APPROVAL COULD COME SOONER DUE TO STRENGTH OF STUDY DATA, BUT HARD TO PREDICT REGULATORY TIMELINES EDWARDS CEO SAYS COMPANY ON TRACK TO SUBMIT FINAL DATA SETS FOR INTERMEDIATE-RISK PATIENTS TO FDA IN NEXT COUPLE OF WEEKS (Reporting by Susan Kelly in Chicago)
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