BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    DP4 Microneedling device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Powered Microneedle Device

    FDA classification
    FDA Class 2 ·Powered Microneedle Device

    C-QUR RPM MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KMTI S141 Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Mesh, Surgical, Polymeric

    FDA classification
    FDA Class 2 ·Mesh, Surgical, Polymeric

    Intervertebral Fusion Device With Bone Graft, Lumbar

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