Next Generation Stent Retriever Receives 510(k) Clearance

CERENOVUS, part of the Johnson & Johnson Medical Devices Companies, announced today it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for EMBOTRAP II Revascularization Device, a next generation stent retriever used to capture and remove life-threatening blood clots from the brain following an ischemic stroke. Stroke strikes nearly 800,000 Americans…

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3D Printed Bone Segments for Foot and Ankle Fixation Receive 510(k) Clearance

Additive Orthopaedics, LLC., the leader in 3D printed orthopaedic foot and ankle devices, today announced that is has received FDA 510(k) clearance for its Patient Specific 3D Printed Bone Segments, to address internal bone fixation in the ankle and foot. According to Greg Kowalczyk, President of Additive Orthopaedics, “This is a tremendous milestone for orthopaedics and…

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Medical Device Companies Could Be Hurt By Chinese Tariffs

US medtech firms, including GE Healthcare (NYSE:GE) and the thriving Minnesota-based medtech sector, are concerned that tariffs on Chinese products proposed by President Trump could significantly affect their business, according to two reports released this week. GE Healthcare executives are worried that the tariffs could hurt the competitiveness of its products, including its magnetic-resonance imaging units which…

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First-in-World Robot-Assisted Spinal Surgery Performed by Penn Neurosurgeons and Otolaryngologists

Noah Pernikoff is back to his life in New York City after becoming the first patient in the world to undergo a complex three-part, robotic-assisted surgery. The robotic arms made it possible for the multidisciplinary team at Penn to successfully remove a rare tumor from Noah’s neck, where the skull meets the spine. The ground breaking…

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First Jellyfish-based biologics manufacturer receives funding

Jellagen, a pioneer in marine biotechnologies based in Wales, has closed a £3.8m funding round led by Newable Private Investing, the Development Bank of Wales, and Angel Investors. Newable Private Investing is one of the UK’s leading private investment groups, providing support to cutting-edge start-ups. As the first commercial manufacturer of next-generation jellyfish collagen for…

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Medtronic’s New 3D Printed Technique to Enhance Surface Textures for Spinal Surgery Implants

DUBLIN and NEW ORLEANS – May 1, 2018 – Medtronic plc (NYSE: MDT) today announced the launch of a titanium 3D printed platform – TiONIC(TM) Technology – that enables more complex designs and integrated surface technologies for spine surgery implants. The announcement was made during the American Association of Neurological Surgeons (AANS) annual meeting in New…

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Former Stryker Engineer Pleads Guilty to Accepting Bribe

Daniel Lawrynowicz, a former Stryker Corporation engineering director, pled guilty on April 3, 2018 to accepting a $75,000 bribe for steering business to a New York metallurgy firm. According to the Department of Justice (DoJ), Lawrynowicz, 48, pleaded guilty before U.S. District Judge Madeline Cox Arleo in Newark federal court to an information charging him…

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World’s first total penis and scrotum transplant performed at Johns Hopkins

Johns Hopkins Medicine

Many soldiers returning from combat bear visible scars, or even lost limbs, caused by blasts from improvised explosive devices, or IEDs. Some servicemen also return with debilitating hidden injuries—the loss of all or part of their genitals. The Johns Hopkins reconstructive surgery team that performed the country’s first bilateral arm transplant in a wounded warrior…

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Graphene spikes on implants can kill harmful bacteria

Photo: Johan Bodell

A tiny layer of graphene flakes becomes a deadly weapon and kills bacteria, stopping infections during procedures such as implant surgery. This is the findings of new research from Chalmers University of Technology, Sweden, recently published in the scientific journal Advanced Materials Interfaces. ​Operations for surgical implants, such as hip and knee replacements or dental…

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FDA Demands Medical Devices to up their Security!

  The US Food & Drug Administration plans to ask Congress for more funding and regulatory powers to improve its approach towards medical device safety, including on the cybersecurity front. An FDA document released this week reveals several of the FDA’s plans, including the desire to force device makers to include mandatory update systems inside…

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