Medical Devices: Page 185


  • Breast health and diagnostics drive Hologic to beat-and-raise quarter

    Double-digit growth by Hologic's core businesses offset ongoing underperformance by its Cynosure medical aesthetics unit.

    By Jan. 31, 2019
  • Baxter beats estimates despite ongoing medication delivery woes

    To drive long-term growth, Baxter is "very aggressively" looking for takeover targets, CEO José Almeida said on an earnings call.

    By Jan. 31, 2019
  • Boston Scientific's Farapulse pulsed field ablation device. Explore the Trendline
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    Permission granted by Boston Scientific
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    Trendline

    New medical devices are reshaping the medtech industry

    From pulsed field ablation devices to glucose sensors and surgical robotics, new medical technologies are transforming patient care and how people manage their health.

    By MedTech Dive staff
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    Cybersecurity device plan seeks alignment of industry, regulators

    A team led by representatives from BD, Mayo Clinic and FDA released a guide on managing the security of medical devices in clinical practice.

    By Jan. 30, 2019
  • Tumbling breast implant sales drag on Allergan's Q4 results

    The loss of a CE mark contributed to a 74% drop in European sales of the devices.

    By Jan. 30, 2019
  • Stryker impresses in Q4, sets bold forecasts

    The Kalamazoo, Michigan-based medical device maker forecast organic sales growth in the range of 6.5% to 7.5% in 2019 that represents its strongest outlook in a decade.

    By Jan. 30, 2019
  • J&J data suggests its stapler reduces more lung surgery air leaks than competitor

    The company pointed to research indicating use of its Ethicon surgical stapler in a lung cancer procedure led to less than half the rate of air leak complications than Medtronic's design did.

    By Jan. 29, 2019
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    Milken Institute
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    FDA sets March date for breast implant panel meeting

    The agency plans to re-examine the benefit-risk profile of the controversial medical devices amid revival of a long-running debate over safety. 

    By Jan. 29, 2019
  • Gottlieb, Shuren tout 2018 as 'record' year for novel devices

    The FDA officials also cited progress with real world evidence, pondered expanding authorities to revamp the 510(k) system and floated creating a fast-track pathway for products addressing non-life-threatening diseases.

    By Maria Rachal • Jan. 29, 2019
  • Philips hits sales targets despite headwinds and patchy performance

    The trade war between the United States and China is taking a toll on the multinational conglomerate.

    By Jan. 29, 2019
  • The FDA logo on a glass pane at the agency's campus in Silver Spring, Maryland.
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    Jacob Bell/MedTech Dive
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    Zimmer Biomet gets 510(k) for robotic knee surgery system

    With the Rosa Knee authorization, the orthopaedics device maker takes on rival Stryker and its Mako robotic platform.

    By Jan. 28, 2019
  • ResMed Q2 revenue miss sends shares plunging

    The maker of sleep apnea and respiratory care devices reported second-quarter revenue that missed analysts' targets, sending its shares plummeting more than 19% Friday.

    By Jan. 28, 2019
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    Draeger Medical recalls single-use breathing circuits

    The accessory works with a ventilator or anesthesia machine and could cause severe oxygen loss or death if the breathing hose short circuits and patients do not receive ventilation.

    By Jan. 28, 2019
  • Medtronic buys Epix to boost cardiac ablation unit

    Terms for the acquisition were not disclosed, but the device giant said the company is pre-revenue and the deal will be dilutive.

    By David Lim • Jan. 25, 2019
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    Varian begins 2019 with guidance-beating quarter

    Strong global demand for radiotherapy devices enabled the Palo Alto-based oncology treatment and software manufacturer to brush off the impact of tariffs.

    By Jan. 25, 2019
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    Fotolia
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    FDA grants breakthrough status to Liberate's ventilator device

    The special designation covers a muscle stimulator designed to wean patients off mechanical ventilation.

    By Jan. 25, 2019
  • Intuitive Surgical to step up investment outside the US

    The maker of the da Vinci robotic system is looking to build its business operations in new markets including China, India and Taiwan.

    By Jan. 25, 2019
  • Boston Scientific rolls out latest DBS systems targeting Parkinson's

    The company said its latest systems are smaller, offer longer battery life and are more customizable than other products on the market.

    By Maria Rachal • Jan. 25, 2019
  • Device lobby pushes bill to let FDA take user fees amid shutdown

    But the proposal does not appear to be poised for movement. Democrats on the House Energy & Commerce Committee oppose the legislation, a Democratic committee staffer told MedTech Dive.

    By David Lim • Jan. 24, 2019
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    Double-digit growth in hip and knee replacements spikes health spending

    The analysis shows a growing proportion of Blue Cross Blue Shield members are electing to undergo the orthopaedic procedures.

    By Jan. 24, 2019
  • Hospitals call on medtech to ease interoperability by boosting security

    "Medical device manufacturers must do more to confront the privacy challenges that unsecurable devices may pose to hospitals and health systems," the American Hospital Association and six other groups said in a report.

    By Meg Bryant • Jan. 23, 2019
  • Medtronic data show no paclitaxel-mortality link amid FDA warnings

    A study of peripheral artery disease patients treated using paclitaxel-coated balloons differed in conclusions from a meta-analysis that prompted an agency safety alert last week.

    By Jan. 23, 2019
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    Milken Institute
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    FDA expands Abbreviated 510(k) guidance, seeks predicate input

    FDA Thursday extended the comment period by 30 days for its request for feedback on its proposal to overhaul the 510(k) program to encourage use of more modern predicate devices.

    By David Lim • Updated April 12, 2019
  • J&J hit with $120M bill in 46-state hip implant marketing settlement

    South Carolina and Texas led the effort alleging Johnson & Johnson mischaracterized the longevity and safety of two DePuy Orthopaedics hip replacement products no longer on the market.

    By Maria Rachal • Jan. 23, 2019
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    Stanford University
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    Illumina TruSight assay gets FDA breakthrough designation

    The DNA sequencing company is seeking clearance of the assay as a companion diagnostic.

    By Jan. 23, 2019
  • Abbott misses sales expectations despite device, diagnostic unit growth

    The medical device unit had the strongest quarter of four divisions, with double-digit growth in sales of diabetes, electrophysiology and structural heart products fueling its performance.

    By Jan. 23, 2019