BEUDAMED
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    SICAT FUNCTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517577450·CoRoent Ant TLIF PEEK, 13x13x32mm 0°

    HHM

    FDA UDI
    Oticon A/S·05707131259912·H110, MINIBTE 312 WL 85 SGR HHM

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365121258·

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365105968·

    SCOUT PRO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTHES XRL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172726·PS Tibia Insert Trial with Posterior Pin Relief...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144808·L UHMWPE PS Tibial Insert Sz B 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523142903·L E-CIMA Vitamin E PS Tibial Insert Sz B 20mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523147212·PS Tibia Insert Trial Size B, 20mm - Left

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523143764·L CIMA HXL PS Tibial Insert Sz B 20mm

    Custom Medical Specialties, Inc.

    FDA UDI
    CUSTOM ASSEMBLIES, INC.·00815849021532·20" LS Extension Set - Sterile

    U-BLADE SET, TI GAMMA3 10.5X100MM

    FDA Adverse Event
    Injury ·STRYKER OSETOSYNTHESIS KIEL·Product code HSB·December 18, 2012

    INSULIN INFUSION PUMP

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

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·May 29, 2013

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 20, 2011

    Boston Scientific Radial Jaw Large Capacity Biopsy Forceps with Needle, Sterile, 240 mm. Box of 20 UPN Number: M00513331 REF: 1333-20

    FDA Recall
    Terminated ·Boston Scientific Corporation·Product code FFF·August 28, 2007

    M2A 1 PC SHELL 38MMX56MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 26, 2016

    M2A 1 PC SHELL 38MMX54MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 26, 2016