BEUDAMED
    11 results · 20ms · 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 ×

    OPAL BOND MV

    FDA 510(k)
    FDA Class 2 ·Dental

    BENCO

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975004833·Orthodontic How Pliers Curved, #111

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450722305·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0140060·Locking Cap, Temporary, Screw to Screw Distractor

    G6PDH, GLUCOSE-6-PHOSHATE DEHYDROGENASE

    FDA 510(k)
    FDA Class 2 ·Hematology

    SELECTA 7000 FREQUENCY DOUBLED, Q-SWITCHED ND:YAG OPHTHALMIC LASER

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 22, 2025

    URETEX SUPPORT PP KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·April 4, 2013

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 16, 2014

    NEURAWRAP NERVE PROTECTOR 7MM ID X 4CM LENGTH

    FDA Adverse Event
    Other ·INTEGRA, PLAINSBORO·Product code JXI·April 27, 2011

    CATH. GUIDE 6F AL 2.0 110CM LA CATHETER LA6AL20A LA 6F 110CM AL20 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. Product Number: LA6AL20A

    FDA Recall
    Terminated ·Medtronic, Inc.·Product code DQY·April 5, 2006