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

    ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring

    FDA 510(k)
    FDA Class 2 ·Dental

    Device, Anti-Snoring

    FDA classification
    FDA Class 2 ·Device, Anti-Snoring

    SURGIFORM AUGMENTATION MATERIAL (S.F.A.M.)

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

    STAXX XD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

    FDA classification
    FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

    Spinal Vertebral Body Replacement Device

    FDA classification
    FDA Class 2 ·Spinal Vertebral Body Replacement Device