BEUDAMED
    175 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    NO-PROFILE SCREWS NO-PROFILE WASHER NO-PROFILE SCREWS WASHERLOC WASHERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857554184·Parallel Trial Size 14x30x9 mm

    UNI KNEE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GMK REVISION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GMK-REVISION FEMUR REVISION PS SIZE 6 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 12, 2017

    GMK-HINGE FIXED TIBIAL TRAY SIZE 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·August 28, 2019

    GMK HINGE FEMUR SIZE 5 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

    GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 25, 2017

    GMK-REVISION FEMUR REVISION PS SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 19, 2019

    GMK HINGE FEMUR SIZE 2 RIGHT

    FDA Adverse Event
    Injury ·Product code KRO·September 12, 2014

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 29, 2025

    GMK-REVISION FEMUR REVISION PS SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 6, 2018

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·December 7, 2017

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 3+ RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 12, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 2, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·October 4, 2017

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 15, 2025

    ADULT VENTILATOR DUAL HEATED CIRCUIT KIT

    FDA Adverse Event
    Malfunction ·Product code BZE·September 10, 2020

    ADULT VENTILATOR DUAL HEATED CIRCUIT KIT

    FDA Adverse Event
    Malfunction ·Product code BZE·December 4, 2020

    GMK-HINGE FIXED TIBIAL TRAY SIZE 4 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·April 7, 2020