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Author: Brenda Fulmer

High Risk Devices Still Not Reclassified

12/13/2012
Articles
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By the end of the year, the U.S. Food and Drug Administration (FDA) had stated it would make sure that high-risk medical devices were approved through the most stringent premarket approval (PMA) review process to assure the safety of consumers. But it looks as though that will not happen. High-risk […]

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Searcy Denney Files New Defective Sling Case

11/26/2012
Mass Torts
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The manufacturers of defective medical devices have been the focus of a number of lawsuits filed by the Mass Tort Unit of Searcy Denney this week. A new lawsuit was filed in the United States District Court for the Middle District of Florida, Tampa Division, against Mentor Worldwide (a Delaware […]

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