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    Neosoma, Inc. a Medical Technology Company Focused on Advancing the Treatment...

    milestones

    MHRA appoints first new UK Approved Body to certify medical devices...

    Mesh Suture receives approval for non-absorbable polypropylene mesh suture

    Seer Medical receives FDA 510(k) for its at-home epilepsy diagnosis aide

    neurology

    Precisis lines up EU approval for ‘brain pacemaker’ to treat epilepsy

    FDA approves DyAnsys’ Primary Relief to treat pain after cardiac surgery

    Stryker’s bone tumour ablation system receives FDA 510(k) clearance

    Magnus’ SAINT Neuromodulation System secures FDA 510(k) clearance

    Viz.ai receives FDA clearance for pulmonary embolism-related algorithm

    Noul obtains CE-IVD marks for two diagnostic testing products

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