BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    ACROMED CANCELLOUS BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556707378·GC Initial™ Zr-FS Dentin DA3, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228750531·GC Initial™ Zr-FS Dentin DA3, 20g

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902278372·RETRACTOR X875-053 CURVED HANDHELD 18MM

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668109540·PETERS HYDRODISSECTION CANNULA 25GA

    SERA-TEK MICROSOMAL ANTIBODY TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    THABEST-IGE

    FDA 510(k)
    FDA Class 2 ·Immunology

    X3 TRIATHLON CS INSERT #3 9MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·June 16, 2014

    FLORENCE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL QUEBEC, LP·Product code FNL·October 13, 2010

    UNKNOWN DEPUY POLY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·December 17, 2012

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024