BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    KIRSCHNER SELF-TAPPING ACETABULAR CUP

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209108534·

    300 Series Facebow

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746150715·FACEBOW LOOP STYLE W/BAYONET 045 SIZE 5 111MM

    Endo-Model SL Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575384099·Modular Stem, with male taper for 6mm noses, ce...

    HDR IORT SHIELDED APPLICATOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    UniSpace® TPLIF Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUMMIT POR TAPER SZ7 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 5, 2014

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·November 13, 2012

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·September 29, 2010

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024