BEUDAMED
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    HEADWAY 17 ADVANCED MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medline Industries, Inc.

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10198459282409·TRAY CHEST TUBE INSERTION DISP

    Oticon

    FDA UDI
    Oticon A/S·05707131165121·K13, BTE 13 P SGR

    AIM™FEMORAL NAIL

    FDA UDI
    Biomet Orthopedics, LLC·00887868003660·

    MicroScan

    FDA UDI
    Beckman Coulter, Inc.·15099590655839·MicroScan 0.05N Sodium Hydroxide - 250ml

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111347047·TRAY COVER FOR 10-1742

    ALLURE® MB

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807101542041·ALLURE® MB SEW .022 UPPER 4&5

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111330418·TRAY COVER FOR 10-1742 PK/12

    SPECIALTY D-UV (OCUFILCON D) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR, SPECIALTY D-UV MULTIFOCAL (OCUFLICON D)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CONSENSUS REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·May 9, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·May 1, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·June 8, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·April 26, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·April 20, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·February 23, 2024

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·May 3, 2013

    S4S/SUR-FIT NATURA 2 PC - 2 PC DURAHESIVE (DH)

    FDA Adverse Event
    Injury ·CONVATEC INC.·Product code EXE·August 19, 2014