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    Waypoint Orthopedics seeks FDA 510(k) approval for smart bone awl

    neurology-neuro-meuspera-medical

    DyAnsys receives US FDA approval for First Relief neurostimulation device

    FDA clears Healthy.io’s smartphone-based AI test for early-stage kidney disease

    Ancora Heart Receives Breakthrough Device Designation from FDA for the AccuCinch® Ventricular Restoration...

    Renovia receives FDA clearance for leva® Pelvic Health System as first-line...

    Ra Medical Systems Receives FDA 510(k) Clearance for the DABRA 2.0...

    ResApp gets 510(k) clearance for mobile sleep apnoea test SleepCheck

    Terumo Aortic Announces First Commercial Implant of the Thoraflex Hybrid Device...

    LiveMetric secures FDA 510(k) clearance for LiveOne BP monitoring system

    US FDA grants expanded 510K clearance for MolecuLight’s i:X imaging device

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