BEUDAMED
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    AI.ME System

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

    Zavation

    FDA UDI
    Zavation LLC·00842166133198·Ti3Z CIF 14mmx16mmx11mm -10 deg

    10PW - Pike Electric

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588210117·10PW - Pike Electric

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193115085·HA PEEK EVOS Straight, ,11mmx8mmx 26mm , BICONV...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946071929·X SERIES, HOSPITAL, MONITOR/DEFIBRILLATOR, 3/5 ...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946072230·X SERIES, HOSPITAL, MONITOR/DEFIBRILLATOR, 12 L...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946097769·X SERIES, MONITOR/DEFIBRILLATOR, EMS, 12 LD W/...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946012649·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946061449·X SERIES, MONITOR/DEFIBRILLATOR, 12 LD W/ INTER...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946014933·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946005979·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946019143·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167322210110·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167312210110·

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946011048·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946018726·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946060060·X SERIES, MONITOR/DEFIBRILLATOR, 3/5 LEAD, ECG,...

    Medtronic Model 5392 External Pulse Generator (EPG)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMISTEM AND QUADRA - LINE EXTENSION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IQ FLEX M

    FDA Adverse Event
    Malfunction ·FIRST SOURCE INC.·Product code IZL·May 29, 2024