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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Aug. 19, 2019

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Profound Medical gets FDA nod to market prostate tissue ablation system

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South Korea's Pcl eyes European market for its tumor marker diagnosis kit

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Coagulation factors shown to be effective against resistant gram-negatives

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Ring remover fingered as solution to cuts and burns at North American hospitals

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Other news to note

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Daily M&A

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BioWorld MedTech stock report for public med-tech companies

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Financings

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Appointments and advancements

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Product clinical data for Aug. 16, 2019

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Product regulatory actions for Aug. 16, 2019

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BioWorld MedTech's Neurology Extra

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FDA gives nod to Edwards, Medtronic TAVR devices for low-risk patients

The U.S. FDA approved four transcatheter aortic valve replacement (TAVR) devices for use in patients at low risk of poor surgical outcomes: two of the Corevalve family from Medtronic plc, of Dublin, and two of the Sapien brand from Edwards Lifesciences Corp., of Irvine, Calif. The news comes roughly eight months after both companies presented data for this patient population at a major medical conference and signals robust growth for this device type for the foreseeable future. Read More

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