BEUDAMED
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    ADVIA CHEMISTRY GLUCOSE HEXOKINASE_3 (GLUH_3) REAGENT, MODELS REF 05001429

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964069987·Endo Carry-On Procedure Kit

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111005824·COVER FOR 10-1750 & 10-1752

    Sklar®

    FDA UDI
    SKLAR CORPORATION·30649111082225·COVER - 10-1750 & 10-1752 PK 6

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111043653·COVER FOR 10-1750&10-1752 PK12

    TOKUYAMA M-BOND

    FDA 510(k)
    FDA Class 2 ·Dental

    PREMIUM PLUS DISPOSABLE PROPHY ANGLE MODEL 3399

    FDA 510(k)
    FDA Class 1 ·Dental

    Widex

    FDA UDI
    Widex A/S·05706069727005·Widex EVOKE E-PA (Tech Black S-110 ) RC coil

    KYPHOPAK TRAY

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·May 24, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·November 6, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·April 5, 2021

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·July 11, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·August 31, 2019

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code HRX·March 7, 2018

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 9, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 19, 2014

    2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011

    KYPHON XPANDER II INFLATABLE BONE TAMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HRX·May 17, 2018

    1030489-2019-01511

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019

    KYPHON XPANDER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code HRX·March 23, 2021