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CMR Surgical Reportedly Exploring $4B Sale

CMR Surgical is reportedly seeking a $4 billion sale, according to the Financial Times. The U.K.-based robotic surgery firm has engaged advisors to explore strategic

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FineHeart Approved for First-In-Human LVAD Study in France

French regulators have authorized FineHeart to begin its first-in-human trial of the FlowMaker, a next-gen left ventricular assist device (LVAD) for advanced heart failure patients.

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J&J MedTech Unveils Kincise 2 for Hip and Knee Surgery

Johnson & Johnson MedTech has launched the Kincise 2, a next-gen automated power tool system designed to enhance surgical control and reduce physical strain during

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Philips Earns CE Mark for SmartCT Stroke Imaging Tech

Philips has secured CE mark approval for its next-gen SmartCT imaging solution, designed to enhance real-time stroke and neurovascular care. Already in use in Japan

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DeviceTalks Minnesota Nearly Sold Out Ahead of June 11 Event

DeviceTalks Minnesota is approaching full capacity, with the June 11 event drawing over 250 medtech professionals to the McNamara Alumni Center. The gathering will feature

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Salvia BioElectronics Raises $60M to Advance Migraine Implant Therapy

Dutch medtech company Salvia BioElectronics secured $60 million in Series B funding to accelerate clinical development and launch of MySalvia Therapy—a neuromodulation treatment using an

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German Bionic Launches Exia: AI-Powered Wearable Exoskeleton

German Bionic unveiled its latest wearable exoskeleton, Exia, featuring advanced AI-driven support designed for diverse labor tasks. Built on billions of real-world motion data points,

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Surgify Medical Raises $7.8M Series A to Advance Bone-Cutting Tech

Helsinki-based Surgify Medical secured $7.8 million (€7 million) in a Series A round led by Zeiss Ventures, with participation from the European Innovation Council Fund

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BD Issues Safety Warning on Esophagogastric Balloon Tamponade Tubes After Death

The FDA highlighted a safety notice from BD and its C.R. Bard subsidiary following one death and two serious injuries linked to esophagogastric balloon tamponade

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AnX Robotica Secures FDA Clearance for Next-Gen GI Motility Capsule

AnX Robotica announced FDA 510(k) clearance for its MotiliCap technology and companion MotiliScan software, marking a leap forward in gastrointestinal (GI) motility monitoring. MotiliCap, a

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