BEUDAMED
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    JBS-LVO

    FDA 510(k)
    FDA Class 2 ·Radiology

    JBS SMOOTH FIXATION PIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ZHONGSHAN A&J MEDICAL EQUIPMENT CO., LTD. (JBS)

    FDA registration
    ZHONGSHAN A&J MEDICAL EQUIPMENT CO., LTD. (JBS)·9 products·🇨🇳 China

    Jet Black Supply

    FDA UDI
    Nexus Brands Group, Inc.·00630148904931·Individual box, X LARGE

    Jet Black Supply

    FDA UDI
    Nexus Brands Group, Inc.·00630148904917·Individual box, MEDIUM

    Jet Black Supply

    FDA UDI
    Nexus Brands Group, Inc.·00630148904900·Individual box, SMALL

    Jet Black Supply

    FDA UDI
    Nexus Brands Group, Inc.·00630148904924·Individual box, LARGE

    10MM TI CANNULATED TIBIAL NAIL-EX/360MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code JDS·August 15, 2017

    SPINE SYSTEM

    FDA Adverse Event
    Injury ·JBS, SA·Product code JBS·August 12, 1996

    SPINE SYSTEM 5

    FDA Adverse Event
    Injury ·JBS SA·Product code JDN·October 2, 1996

    SPINE SYSTEM 5 IMPLANTS

    FDA Adverse Event
    Injury ·JBS, SA·Product code MCV·October 11, 1996

    SPINE SYSTEM 5 ROD, TITANIUM ALLOY, 150MM

    FDA Adverse Event
    Malfunction ·AESCULAP - JBS S.A.·Product code MNH·May 13, 1999

    SPINE SYSTEM 5 PEDICLE SCREW

    FDA Adverse Event
    Injury ·AESCULAP JBS, SA·Product code MCV·November 15, 1996

    SPINE SYSTEM IMPLANTS

    FDA Adverse Event
    Injury ·AESCULAP/JBS SA·Product code KWP·March 25, 1997

    SPINE SYSTEM ROD, TITANIUM ALLOY

    FDA Adverse Event
    Injury ·AESCULAP - JBS S.A.·Product code KWP·September 16, 1999

    SPINE SYSTEM SCREWS

    FDA Adverse Event
    Injury ·AESCULAP/JBS SA·Product code JDN·November 3, 1997

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 23, 2026

    MENTOR SMOOTH ROUND HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·April 24, 2019

    MENTOR SMOOTH ROUND HIGH PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·April 24, 2019

    UNK - IMPLANT

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code HWC·April 7, 2026