BEUDAMED
    25 results · 24ms · Sources: EU EUDAMED, US FDA

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    Stryker Spine Navigation System with SpineMap 3D software application, OrthoLock, nGenius Spine Clamp, Navigated Drill Guide Set, Navigated Xia 3 Awl Tap, Navigated Xia 3 Serrato Tap

    FDA 510(k)
    FDA Class 2 ·Neurology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027106·2.0mm X 34mm Cannulated Headless Screw

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023119·Female Post, 2 Hole

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036821·Trial Rasp, No Stop, Assembly, Lordotic, 6mm

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036883·Trial Rasp, No Stop, Assembly, Lordotic, 12mm

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036852·Trial Rasp, No Stop, Assembly, Lordotic, 9mm

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036876·Trial Rasp, No Stop, Assembly, Lordotic, 11mm

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036838·Trial Rasp, No Stop, Assembly, Lordotic, 7mm

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036869·Trial Rasp, No Stop, Assembly, Lordotic, 10mm

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036845·Trial Rasp, No Stop, Assembly, Lordotic, 8mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031714·2.0mm x 34mm Headless Screw, Sterile

    Arena-C®

    FDA UDI
    SPINEFRONTIER, INC.·00190361036814·Trial Rasp, No Stop, Assembly, Lordotic, 5mm

    BLUE SKY BIO DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    DIODE MEDICAL LASER FAMILY, MODELS 4, 6, 30

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068642·Cannulated 2.0 x 34mm Headless Screw Sterile Qty 5

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·KANAE CO.,LTD.·Product code KDJ·June 17, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 18, 2008

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023