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MedTech Dive
网络媒体
Washington，District of Columbia 16,804 位关注者
Business journalism and in-depth insight into news and trends shaping medical technology
关于我们
MedTech Dive brings you in-depth journalism and insight into the news and trends shaping the business of medical technology. Subscribe for our free daily newsletter to learn about medical devices, diagnostics, M&A, digital health, FDA regulation/compliance, R&D, imaging and more. MedTech Dive is published by Industry Dive. Our business journalists spark ideas and shape agendas for 13+ million decision-makers.
- 网站
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https://www.medtechdive.com/signup/
MedTech Dive的外部链接
- 所属行业
- 网络媒体
- 规模
- 201-500 人
- 总部
- Washington，District of Columbia
- 创立
- 2018
- 领域
- Medical Technology, medical devices, medical imaging, diabetes technology
动态
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ICU Medical's Smiths Medical business?recalled ProPort implantable ports?because of a manufacturing defect. Separately, the company warned of a tube size problem with some oral/nasal endotracheal tubes.
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The Food and Drug Administration?posted?an early alert about an issue?with Calyxo, Inc.’s CVAC aspiration systems linked to one death.
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GE HealthCare, Synchron and robotics companies were among the medtech firms that used NVIDIA's GTC 2025 conference to share updates on their work with the AI computing leader.
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Mark Field, Insulet Corporation's chief technology officer, left the company on Friday to pursue other opportunities. Amit Guliani, Insulet’s group vice president of software engineering, became acting CTO. https://lnkd.in/gyKBCH74
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At the first day of #ATTD25, Dexcom previewed new data for its 15-day continuous glucose monitor, and Tandem Diabetes Care shared results of a pivotal trial of its Control-IQ+ algorithm for Type 2 diabetes. https://lnkd.in/gzFQ3r4p
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Medtronic has recalled?embolization devices collectively linked to reports of 17 injuries and four deaths, the Food and Drug Administration said Tuesday.
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Monogram Technologies secured 510(k) clearance for its robotic knee replacement system. Meanwhile, robot developer Vicarious Surgical Inc. said supply chain issues delayed its regulatory timeline.
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Spectral AI Deepview System?has outperformed?burn physicians in identifying non-healing tissue.
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Many reports of medical device adverse events are sent to the FDA later than the 30-day requirement, according to a?study published in the BMJ. Just 71% of adverse events were reported on time, according to the study. About 15.5% of reports had missing or invalid date data. https://lnkd.in/gDgZGxZV