BEUDAMED
    8 results · 19ms · 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.

    LAVAGING CATHETERS

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

    Tranquil-L™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788220610·Posterior Interbody Trial 16x9x28

    K-Y BRAND LIQUIBEADS

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

    CVSI PERIPHERAL BALLOON CATHETER; CVSI INFLATER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2A-MAGNUM MOD HD SZ 42MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 20, 2014

    VERSAPORT V2 FIXATION CANNULA 12MM

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC·Product code GCJ·October 9, 2012

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code MTA·August 24, 2010

    ACCOLADE SR SL MRI (Model L310)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025