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BioWorld - Thursday, February 26, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Oct. 15, 2015

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Nanoknife approved in S. Korea: Angiodynamics looks to overcome Q1 adversity in the second half

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Clash of Social Media/Science: Social media is a breeding ground of threats for clinical trials

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Inside the Beltway: IBM's Merge fails to report recall for instrument malfunctions

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Agreements/contracts: Novation works with Medline for medical device reprocessing

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Patent watch: Glytec allowed application for diabetes management technology

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Hit Bits: Medhelp launches solution for research, patient engagement

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TCT notebook: Medtronic gets positive Corevalve results in new patient populations

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Financings: Greatbatch to sell $360M of notes for Lake Region deal

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People

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product briefs

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Products

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MDD's Ortopedics Extra

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Transcatheter Cardiovascular Therapeutics Conference: Tryton Medical meets primary endpoint in study, prepares to file for FDA approval

SAN FRANCISCO — Tryton Medical (Durham, N.C.), a private company, reported it has met its primary endpoints from a pivotal confirmatory study surrounding the acceptable acute safety profile of the Tryton Side Branch Stent for the treatment of coronary bifurcation lesions in vessels appropriate for a ≥2.5mm stent. Results of the study were presented as part of the featured here at the clinical research session at the Transcatheter Cardiovascular Therapeutics (TCT) conference. Read More

Heartflow stands tall on PLATFORM study results

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