BEUDAMED
    35 results · 23ms · Sources: EU EUDAMED, US FDA

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    MOTOTM Partial Knee & MOTO PFJ Systems Extension

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MOTO PARTIAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·November 4, 2025

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/14 MM R E-CROSS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 29, 2023

    MOTO PFJ SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·October 1, 2025

    MOTO PARTIAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·April 23, 2026

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 31, 2025

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 27, 2025

    MOTO PFJ SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·May 28, 2026

    MOTO PARTIAL KNEE SYSTEM - MEDIAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·April 14, 2026

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 18, 2025

    MOTO PARTIAL KNEE SYSTEM - MEDIAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·April 30, 2026

    MOTO PARTIAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·November 10, 2025

    GMK PRIMARY TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 6, 2025

    MOTO PARTIAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·May 22, 2026

    MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 RM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·March 8, 2024

    SECURCUT ASPIRATION BIOPSY NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SYNTHECEL DURA REPLACEMENT DEVICES

    FDA 510(k)
    FDA Class 2 ·Neurology

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 23, 2008

    ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 16, 2011

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 9, 2013