BEUDAMED
    16 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 ×

    speX Support Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074520711·SPACER 9193012 CRESCENT PEEK 30X12

    ECHO BI-METRIC MICROPLASTY HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304697799·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009799·3.0mm x 12mm Cannulated Lag Screw

    CETRA

    FDA UDI
    Orthofix US LLC·18257200120741·4.0MM X 12MM PRIMARY CONSTRAINED SELF-TAPPING S...

    9.3MHZ PENCIL PROBE SHIELDED

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787021530·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694071062·Cannulated 3.0 x 12mm Lag Screw Sterile Qty 5

    PROMOS MODULAR SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXACTECH BIOLOXDELTA / BIOLOX FEMORAL HEADS, 28MM OD, 32MM OD, 36MM OD, EXACTECH BIOLOX OPTION ADAPTERS/FEMORAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Versa-FX®

    FDA UDI
    Zimmer, Inc.·00889024036130·

    Versa-FX®

    FDA UDI
    Zimmer, Inc.·00889024036147·

    Versa-FX®

    FDA UDI
    Zimmer, Inc.·00889024036123·

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 13, 2008

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code FWM·June 25, 2008

    Olympus Sterile Optical Laser Fiber, single use and reusable

    FDA Enforcement
    Class II ·Terminated·Quanta System, S.p.A.·June 16, 2021