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    JDI ELECTRONICS FACTORY

    FDA registration
    JDI ELECTRONICS FACTORY·7 products·🇨🇳 China

    C-STEM SZ1 (JDI)

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·September 29, 2014

    SOCLEAN 2

    FDA Adverse Event
    Injury ·SOCLEAN, INC.·Product code LRJ·November 12, 2021

    UNKNOWN SHELL IMPLANT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·September 26, 2017

    EXETER V40 STEM 37.5MM NO 1

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CAEN, BENOIST GIRARD & CIE S.C.A.·Product code KWY·February 5, 2010

    JAPANESE OMNIFIT EON CS 127 NKSIZE 6 STEM 30 M

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS·Product code JDI·February 5, 2010

    V40 COCR LFIT HEAD 36MM/0

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK·Product code JDI·March 5, 2010

    EXETER V40 STEM 35.5 MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CAEN, BENOIST GIRARD & CIE S.C.A.·Product code JDI·February 5, 2010

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    OMNIFIT HFX HIP STEM SIZE #08 132

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS·Product code JDI·February 5, 2010

    ALUMINA V40-FEMORAL HEAD 32MM, +0MM NK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK, STRYKER ORTHOPAEDICS·Product code LZO·February 5, 2010

    EXETER V40 STEM 35.5MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CAEN, BENOIST GIRARD & CIE S.C.A.·Product code KWY·February 5, 2010

    ALUMINA V40-FEMORAL HEAD 28MM, +0MM NK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK, STRYKER ORTHOPAEDICS·Product code KWY·February 5, 2010

    TRIDENT 10EDG X3 INSERT 36MM ID

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS·Product code JDI·February 5, 2010

    EXETER X-CHANGE BONE PLUG 10MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code JDI·February 5, 2010

    EXETER FEMORAL HEAD 28M DIA STANDARD NECK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CAEN, BENOIST GIRARD & CIE S.C.A.·Product code JDI·February 5, 2010

    PRMRS NCK STEM TI BM SZ 24 RSA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWY·April 13, 2018

    EXETER FEMORAL HEAD 28MM DIA. STANDARD NECK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CAEN, BENOIST GIRARD & CIA S.C.A.·Product code JDI·February 5, 2010

    C-TAPER COCR LFIT HEAD 26MM/0

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS·Product code JDI·February 5, 2010

    ALUMINA V40-FEMORAL HEAD 36MM, +5MM NK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK STRYKER ORTHOPAEDICS·Product code LZO·February 5, 2010