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

    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

    FDA1

    FDA Approves Pascal TEER Device for Degenerative MR

    Tasso receives FDA 510(k) for patch-like home blood collection device

    FDA Grants Breakthrough Device Designation for CurveBeam AI’s OssView™ Bone Fragility...

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

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