BEUDAMED
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    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981205362·Trial, 9mm x 24mm x 10mm, 15 Deg

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981286330·Interbody, 9mm x 24mm x 10mm, 15 Deg, 3D

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981191221·Interbody, 9mm x 24mm x 10mm, 15 Deg

    WaveForm™ TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981234683·Interbody, 9mm x 24mm x 10mm, 15 Deg, 3D

    V-TREND TARGET RF TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    VELOPEX AQUACUT FLUID ABRASION UNIT

    FDA 510(k)
    FDA Class 2 ·Dental

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·January 22, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014