BEUDAMED
    10 results · 30ms · 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 ×

    SIGNAFUSE Bioactive Bone Graft

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198321·AK3 PS Insert Trial Size 5, 13mm

    CETRA

    FDA UDI
    Orthofix US LLC·18257200134588·4.0mm X 13mm PRIMARY CONSTRAINED SELF-TAPPING S...

    LATERAL SUPERIOR CLAVICLE PLATE, LEFT AND RIGHT; MIDSHAFT SUPERIOR CLAVICLE PLATE, LEFT AND RIGHT; ANTERIOR CLAVICLE PLA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IDUO BICOMPARTMENTAL KNEE REPAIR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·June 9, 2025

    BD BBL¿ TRYPTICASE SOY AGAR WITH 5% SHEEP BLOOD (TSA II)

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·October 7, 2021

    SET SCREWDRIVER, FLEXIBLE SHAFT 4 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·October 8, 2008

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·July 13, 2011

    STORZ

    FDA Adverse Event
    Injury ·KARL STORZ·Product code HET·June 20, 2013