BEUDAMED
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    THE ZIMMER TMT TRABECULAR METAL VERTEBRAL BODY REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809844191·FOR MEN 20-30 MM HG KNEE HIGH CLOSED TOE LARGE ...

    MINIPHYSIONIZER 2.0 AND ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MODIFICATION TO: MEDRAD SPECTRIS SOLARIS MR INJECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® FA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    JUVEDERM (VOLUME/CONCENTRATION UNK)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·April 5, 2013

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·May 27, 2008

    HARMONIC SCALPEL

    FDA Adverse Event
    Malfunction ·ETHICON·Product code LFL·April 8, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 360 mm, Item Number: 814309360

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 19, 2018