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    AESCULAP AG

    FDA registration
    AESCULAP AG·412 products·🇩🇪 Germany

    AS COLUMBUS REV F TIB.OFFSET CEMENT.T1

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·August 27, 2025

    AS COLUMBUS TIB.HEMI-SP.T1/1+ 5MM RL/LM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·August 27, 2025

    AS COLUMBUS REV FEM.SPACER POST.F3 5MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·August 27, 2025

    AS ENDURO FEMORAL COMPONENT CEMENTED F2L

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code KRO·January 24, 2024

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    AVM MICROCLIP PHYNOX CVD.2MM STERILE

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code HCH·January 2, 2024

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    UNKNOWN COMPONENT AESCULAP AG KNEE IMPLANT

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 30, 2026

    COMPONENT OF AN UNKNOWN AESCULAP AG KNEE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·February 26, 2026

    AS TIBIA EXTENSION STEM 10X52MM CEMENTED

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·April 30, 2026

    VEGA PS+ GLIDING SURFACE T2/2+ 14MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·April 30, 2026

    AS VEGA PS TIBIAL PLATEAU CEMENTED T2+

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·April 30, 2026

    S4 SET SCREW NEW VERSION

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code MNI·July 2, 2025

    SHAFT ONLY F/MODULAR MONOPOL.ELECTR

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·August 7, 2025

    S4 POLYAXIAL SCREW 6.0X55MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code MNI·July 2, 2025

    S4 POLYAXIAL SCREW 6.0X55MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code MNI·July 2, 2025

    UNKNOWN COMPONENT AESCULAP AG VEGA KNEE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 10, 2026

    S4 POLYAXIAL SCREW 6.0X60MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code MNI·July 2, 2025