BEUDAMED
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    PREMIER SELF-ETCHING ENAMEL SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040120682·DOUBLE-GUIDED PALATAL EXPANSION SCREWS

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QJR·April 7, 2022

    WHITE KNIGHT BLUE, GREEN FACE MASK, (4 MODELS)

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

    MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX

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

    AUTO SUTURE ENDO UNIVERSAL 65-4.0

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORPORATION·Product code GCJ·September 19, 1997

    INFUSAID IMPLANTABLE INFUSION PUMP

    FDA Adverse Event
    Death ·STRATO/INFUSAID, INC.·Product code MDY·June 13, 1997

    SERIES TEN THOUSAND COMPACT

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·December 9, 1997

    SERIES TEN THOUSAND COMPACT

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·December 9, 1997

    SERIES TEN THOUSAND COMPACT

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·December 9, 1997

    LIFEPORT

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·April 15, 1999

    SYNCHROMED

    FDA Adverse Event
    Other ·MEDTRONIC, INC.·Product code LKK·March 26, 1999

    SYNCHROMED

    FDA Adverse Event
    Other ·MEDTRONIC INC.·Product code LKK·January 10, 2001

    CRYOVALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·October 7, 1998

    Cook

    FDA UDI
    COOK INCORPORATED·00827002107144·Coaxial Disposable Franseen Biopsy Needle

    ENDURON 10D 58 OR 70ODX28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·March 9, 2010

    TESTPACK +2 URINE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JHJ·May 23, 1997

    TEC 6

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code CAD·May 7, 2004

    TEC 6

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code CAD·May 24, 2005

    ELECTRIC DERMATOME HANDPIECE

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code GFD·August 15, 2013