BEUDAMED
    173 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.

    BLUESHINE'S GOLD SERIES

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

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902096204·ADAPTER 9110375 SIZING TPRD 16MM

    Humeris Shoulder

    FDA UDI
    FX SOLUTIONS·03701037306789·STOP DRILL BIT Ø7.5 mm L.150 mm/AO

    MIS C1

    FDA UDI
    MIS Implants Technologies Ltd.·07290108992106·C1 coni con implant D3.75 L10mm, SP

    AOS TIBIAL NAIL 10mm x 37.5cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016161·

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306816192·Steinhauser Bone Holding Forceps: 13cm/5.25in

    Apex

    FDA UDI
    ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529584696·Apex Tibial Nail Ø 11 x 375mm

    TRIMED X-FIX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIMENSION VISTA LOCI CA 19-9 FLEX REAGENT CARTRIDGE, AND DIMENSION LOCI7 CALIBRATOR WITH MODEL(S) K6457, AND KC604

    FDA 510(k)
    FDA Class 2 ·Immunology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 7, 2025

    MONOSYN VIOLET 5/0 (1) 70CM HR17 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·December 11, 2019

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·November 4, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·November 4, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·October 30, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·November 12, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·December 18, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·November 12, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·October 29, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·November 20, 2025

    C1-10375

    FDA Adverse Event
    Injury ·MIS IMPLANTS TECHNOLOGIES LTD.·Product code DZE·November 12, 2025