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BioWorld - Saturday, January 10, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Sep. 26, 2014

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Boston Scientific hoping REPRISE III data leads to FDA approval for Lotus

Boston Scientific (Natick, Massachusetts) has initiated the REPRISE III clinical trial, a pivotal study to evaluate the safety and effectiveness of the Lotus Valve System in patients with severe aortic stenosis and who are considered to be at either high or extreme risk for surgical valve replacement. The Lotus Valve System is a transcatheter aortic valve replacement (TAVR) device that is both fully repositionable and retrievable prior to release. Read More

3DIcon to pursue NIH grant for volumetric imaging technology

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Inside the Beltway: Judge dismisses FDA qui tam lawsuit for lack of jurisdiction

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Financings: Orthofix continues with completing filings of restated financial statements

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With five decades under its belt, Vygon still remains innovative

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Daily M&A: LabCorp to acquire LipoScience for enterprise value of $63 million

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New Ventures: Axio Research launches new Statistical Genetics and Genomics services division

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World in Review: Taiwanese researchers discovers protein in cancer metastasis

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Agreements/conracts: Thermo Fisher, GSK, Pfizer look into NGS oncology testing

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