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BioWorld - Friday, December 26, 2025
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Jan. 11, 2017

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Abbvie backs GMI to sequence 45K genomes

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Jenavalve continues to define role in TAVR space, gears up for its pivotal trial approval

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Bayer, Leica to develop RNAscope-based companion diagnostics

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Daily M&A

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Financings

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Appointments and advancements

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Product briefs

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Other news to note

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MDD's Oncology Extra

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Boston Scientific puts edge back in Lotus, plans continue for FDA approval

SAN FRANCISCO – Boston Scientific Corp. said its bid to bring its Lotus Edge transcatheter aortic valve technology (TAVR) to the U.S. will continue as planned. During a Tuesday breakout session at the 35th annual J.P. Morgan Healthcare conference, the company said the issue had been resolved. Boston Scientific also noted it wasn't a design flaw in the device nor were there any safety issues. The firm said a fix to Lotus Edge required a combination of "minor process and specification changes", rather than any meaningful, costly and lengthy product redesigns. Read More

Dexcom readies for no-fingerstick launch as it preps next-gen, disposables with Verily

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