BEUDAMED
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    TENSYN BAND

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741318500·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674131850060·

    Prestige® Orthopaedic

    FDA UDI
    INNOVATIVE HEALTHCARE CORPORATION·10813172022391·Gloves, Surgical, Latex, Powder-Free, Textured,...

    Oticon

    FDA UDI
    Oticon A/S·05707131259004·NERA PRO, KIT 312 WL DIR L H BE

    NA

    FDA UDI
    Yeti Dentalprodukte GmbH·EYET6131850·Bite Wax Sticks hard pink strawberry 1850g

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587C13185040·13mm H x 18mm W x 50mm L x 4 degree XLIF Corona...

    Freedom Pedicle Screw System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215027261·

    DURASIS DURAL SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPACELABS BLEASESIRIUS ANESTHESIA WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 29, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 20, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 14, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 6, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·October 5, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·September 28, 2021