BEUDAMED
    9 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 ×

    EXCEL REGULAR SET

    FDA 510(k)
    FDA Class 2 ·Dental

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228751411·GC Initial™ Zr-FS Inside IN-41 Flamingo, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556708399·GC Initial™ Zr-FS Inside IN-41 Flamingo, 20g

    ANGIOMED FINE NEEDLES AND NEEDLE SET

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    URESIL T-SYSTEM BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROLITE MESH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·May 1, 2014

    ENTRUST AT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·October 19, 2010

    CONTINUUM SHELL WITH MULTI HOLES

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LZO·December 12, 2012

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

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