FDA launches digital health pilot centred on chronic disease
The US Food and Drug Administration (FDA) has launched Technology-Enabled Meaningful Patient Outcomes (TEMPO), a pilot that aims to promote …
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Conmed to exit gastroenterology business
US-based Conmed is exiting its gastroenterology business, reflecting the company’s aim to sharpen its focus on higher growth margin business …
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Singapore HSA approves Respiree’s 1Bio AI-Acute toolbox
Singapore Health Sciences Authority (HSA) has granted approval for Respiree’s 1Bio AI-Acute toolbox, classifying it as a Class B software-as-a-medical …
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How next-gen medical textiles combine comfort, safety, and sustainability
Every year, millions of disposable gowns end up in medical waste incinerators. But a new generation of sustainable textiles is …
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Natera purchases Foresight Diagnostics
Cell-free DNA and precision medicine company Natera has acquired Foresight Diagnostics, a business known for its ultrasensitive molecular residual disease …
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Cardiawave secures CE mark for ultrasound aortic stenosis therapy
French medtech company Cardiawave has gained an EU CE mark for its non-invasive ultrasound therapy (NIUT) Valvosoft, marking the first …
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The medtech industry in 2026 – new issue of Medical Technology out now
As we head into the new year, now is the time to reflect on activity in the medical device space …
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FDA clears Insulet’s Omnipod 5 algorithm enhancements
Insulet has secured US Food and Drug Administration (FDA) clearance for an algorithm advancement within its Omnipod 5 automated insulin …
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Testmate and Intermountain Health partner for STI testing in US
Testmate Health and Intermountain Health have entered a strategic collaboration and investment agreement to expedite the accessibility of rapid, …
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Atraverse gains FDA clearance for HOTWIRE transseptal access system
Atraverse Medical’s fully integrated HOTWIRE transseptal access system has obtained the US Food and Drug Administration’s (FDA) 510(k) clearance. The system …
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MED-EL’s cochlear implants secure expanded approval in infants
The US Food and Drug Administration (FDA) has approved an expanded indication for MED-EL’s SYNCHRONY cochlea implants in infants aged …
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Medical Device Network Excellence Awards 2025: Husky Technologies™
Husky Technologies™ plays a significant role in medical injection molding, combining precision tooling, integrated systems, and data-driven service into a cohesive …
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Why the right steel is essential for microtome sectioning
Found in laboratories, hospitals, and universities worldwide, a microtome blade is a precise instrument that cuts paper-thin sections of tissue …
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GE HealthCare and URMC forge Care Alliance initiative
GE HealthCare and the University of Rochester Medical Center (URMC) have announced a Care Alliance, an initiative to advance healthcare …
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FDA grants IDE approval for Renerva’s trial of nerve capping device
The US Food and Drug Administration (FDA) has granted investigational device exemption (IDE) approval for Renerva to initiate the first …
