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BioWorld - Wednesday, February 4, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

March 24, 2017

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Biostable Science & Engineering scores FDA nod for aortic valve repair device

Biostable Science & Engineering Inc. received FDA clearance for its Haart 300 product, an annuloplasty device designed for aortic valve repair. The Austin, Texas-based company said it will launch the device in select heart centers this summer. The company has had CE mark for the Haart 300 since March 2016. (See Medical Device Daily, March 9, 2016.) Read More

Big medical device players navigating innovative paths to success in 2017

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Pathologists ink error-based validation scheme for NGS oncology sequencing

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Autoric remote ischemic conditioning device is winning investors' hearts and money

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Appointments and advancements

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Regulatory front

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Product briefs

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Other news to note

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Daily M&A

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MDD's Diagnostics Extra

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