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    Life Spine Gains FDA 510(k) Clearance for PROLIFT Lateral HELO Fixation

    Pixee Medical Receives FDA Clearance for Knee+

    Cerus Endovascular Announces IDE Approval from the U.S. FDA to Conduct...

    Zimmer Biomet Secures FDA Clearance for ROSA® Partial Knee System

    AngioDynamics Submits 510(k) Application to FDA for AlphaVac Mechanical Thrombectomy System

    Chemence Medical’s redesigned skin closure system approved by FDA

    Empirical Spine Receives FDA Breakthrough Device Designation for the LimiFlex Device...

    Digital X-ray company Nanox scores first FDA clearance

    FDA grants Oxehealth Vital Signs De Novo clearance; Oxehealth launches in...

    FDA Grants Breakthrough Device Designation to Tempus’ Atrial Fibrillation ECG Analysis...

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