BEUDAMED
    4 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHARP BRAND ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Needle, Acupuncture, Single Use

    FDA classification
    FDA Class 2 ·Needle, Acupuncture, Single Use