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

    IPL + Diode Laser Machine

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

    Intense Pulsed Light Equipment

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

    CO2 Laser System

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

    Diode Laser Therapy Machine

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

    CO2 Laser Equipment

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

    ND:YAG Laser

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

    US 450 Diode Laser Equipment

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

    Button Loop

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    High Strength Suture

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

    VOLK DISPOSABLE VITRECTOMY LENSES, MODELS VOLK FLAT SSV D, VOLK AFX SSV D, VOLK 45 PRISM SSV D

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    InSpace Subacromial Tissue Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoLink Plating System, Fracture and Correction System, CoLink Mini Plating System, CoLink View Plating System, CoLink Afx Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·INTER FIX THREADED FUSION DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·VISTA LORDOTIC INTERBODY FUSION CAGE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·RAY TFC DEVICE/RAY TFC UNITE DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM