BEUDAMED
    31 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.
    Filters Regulation: Us FDA ×

    LIVER TAMPONADE BALLOON

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

    Vivid Surebond VII

    FDA UDI
    PEARSON DENTAL SUPPLIES, INC.·D724D0104501·

    CORTICAL SCREW 3.5mm x 45.0mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019780·

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0104000·Caddie, Cages, Universal

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0104000·Caddie, Tulip Connectors

    TiWAVE L Lumbar Cage System

    FDA UDI
    Kalitec Direct LLC·BO7323K0104000·Caddie, Trials

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0104100·Caddie Lid, Tulip and Domino Connectors

    PUMA-G System™

    FDA UDI
    Coaptech, Inc.·00850026037227·Percutaneous Ultrasound Gastrostomy (PUG) Syste...

    AUTO SUTURE MICRO SURGICLIP CLIP APPLIER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MODIFICATION TO SYNTHES USS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALTEON

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code MEH·June 8, 2020

    ALT HA S CLR STD SZ 5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code MEH·July 16, 2024

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    ALT XLE LNR NTRL G4 36

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·April 21, 2026

    ALTEON HIP COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·April 27, 2026

    ALTEON

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·March 31, 2026

    ALTEON HIP COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·April 27, 2026

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007

    LARYNGOSCOPE HANDLE

    FDA Adverse Event
    Malfunction ·NEWMATIC MEDICAL·Product code CCW·March 14, 2013

    SOFTCLIX® PLUS LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 8, 2011