BEUDAMED
    7 results · 25ms · 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.

    ARTHROSTRESS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Shepard, Insemi-Cath, and Soft-Pass Coaxial - Cook Intrauterine Insemination Catheters

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BIOFLEX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CORIN BIPOLAR

    FDA Adverse Event
    Other ·CORIN LTD.·Product code KWY·March 17, 2014

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·October 4, 2012

    SERIES 20000 LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 23, 2010

    Unity Total Knee System. Used for knee prosthesis in total knee replacement

    FDA Recall
    Terminated ·Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom·Product code JWH·October 31, 2022