BEUDAMED
    769 results · 22ms · Sources: EU EUDAMED, US FDA

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    ARx Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GoPLF! Posterior Lateral Fusion Device

    FDA UDI
    GetSet Surgical SA·07640387660218·GoPLF! Posterior Lateral Fusion Device, 5.5mm x...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694010917·Lag Screw VISIDISK

    CorticaLINK MI

    FDA UDI
    LINKSPINE, INC.·00817329023043·5.0mm Cobalt Chrome Rod: 70mm Curved

    Insurgical, Inc.

    FDA UDI
    Insurgical, Inc.·00860007230066·2.0 - 3.2 Pin Driver Assembly

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2522000700·Straight Titanium Rod

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555252200070·Taurus Pedicle Screw System- Straight Rod 5.5x70mm

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102200070·Straight Rod 6.0mm, 70mm

    FLOCATH

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

    JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002

    FDA 510(k)
    FDA Class 2 ·Dental

    Widex

    FDA UDI
    Widex A/S·05706069689402·Widex BEYOND B-F2 (Copper brown ) Telecoil, RC ...

    SMR SHOULDER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·August 29, 2025

    DELTA BURR HOLE 16MM, LEV 1.5

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·July 1, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021