BEUDAMED
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    RESURFX 1565NM LASER MODULE

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694025669·Plate, Left L, 8 hole, 1.6mm

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707010012·CALIBRA 1ST MOLAR BANDS n.UL 28

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376610689·Universal Variable Medial Cross Connector, 28mm...

    CPC BY SORING GMBH

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

    EEVATM PETRI DISH

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·ALGOVITA SPINAL CORD STIMULATION SYSTEM

    Widex

    FDA UDI
    Widex A/S·05706069888775·WIDEX MOMENT M-CIC (Clay brown ) 330, Right

    Widex

    FDA UDI
    Widex A/S·05706069558333·Widex UNIQUE U-XP (Clay brown ) 330, Telecoil, ...

    Widex

    FDA UDI
    Widex A/S·05706069886900·WIDEX MOMENT M-XP (Clay brown ) 330, Telecoil

    Widex

    FDA UDI
    Widex A/S·05706069560107·Widex UNIQUE U-CIC (Clay brown ) 330, Right, RC...

    Widex

    FDA UDI
    Widex A/S·05706069673180·Widex EVOKE E-CIC (Clay brown ) 330, Right, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069520057·Widex D-XP (Clay brown ) Dream 330, Telecoil, R...

    Widex

    FDA UDI
    Widex A/S·05706069520149·Widex D-CIC (Clay brown ) Dream 330, Right, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069670424·Widex EVOKE E-XP (Clay brown ) 330, Telecoil, R...

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017