BEUDAMED
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    SAGE 2200 STERILE SPECIMEN CONTAINER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517369307·CoRoent LO Trial, 8x10x40mm 5°

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0134080·Trial, TLIF, 27L OB STR 7Deg, 8mm

    AT HOME DRUG TEST, MODEL 9079

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Q. FREEZE (MOTION VUE2)

    FDA 510(k)
    FDA Class 2 ·Radiology

    SIGMA 300 DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·October 31, 2012

    UNKNOWN TIMESH

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRS·May 15, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·August 19, 2010

    ANATOMICAL SHOULDER¿¢ DOMELOCK®, DOME, CENTRIC

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 21, 2023

    ANATOMICAL SHOULDER¿¢, GLENOID, PEGGED, CEMENTED, M

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 20, 2023

    ANATOMICAL SHOULDER¿¢, HUMERAL STEM, UNCEMENTED, ø 10.5, 100 MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·June 20, 2023