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Cardiology Homepage

Boston Scientific receives FDA approval for LOTUS Edge Aortic Valve System

FDA grants first-ever clearances to detect bradycardia and tachycardia on a personal ECG device

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iSchemaView’s RAPID approved for use in the Kingdom of Saudi Arabia

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Avinger (AVGR) announces receipt of FDA 510(k) clearance of Pantheris SV device

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Insera earns CE Mark approval for cyclical-suction stroke thrombectomy platform, the CLEAR aspiration system

Neovasc announces dismissal of claim brought by Edwards Lifesciences

Press releases may be edited for formatting or style
VANCOUVER, Jan. 22, 2019 /PRNewswire/ - Neovasc Inc. ("Neovasc" or the "Company") (NASDAQ: NVCN) (TSX:NVCN), a leader in the development of minimally invasive transcatheter mitral valve replacement technologies and in the development of minimally invasive devices for the treatment of refractory angina, today announced that, pursuant to a settlement reached with Edwards Lifesciences PVT, Inc. and Edwards Lifesciences (Canada) Inc. (collectively, "Edwards"), the patent infringement action that Edwards had previously commenced in the Federal Court of Canada against Neovasc, Boston Scientific and Livanova, will be dismissed on a no-costs basis.


About Neovasc Inc.
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Neovasc is a specialty medical device company that develops, manufactures and markets products for the rapidly growing cardiovascular marketplace. Its products include the Neovasc Reducer™ (the "Reducer"), for the treatment of refractory angina, which is not currently commercially available in the United States and has been commercially available in Europe since 2015, and the Tiara™, for the transcatheter treatment of mitral valve disease, which is currently under clinical investigation in the United States, Canada and Europe.


SOURCE Neovasc Inc.

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