BEUDAMED
    11 results · 27ms · 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 ×

    ADD-A-SHIELD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707034025·WEB 1ST MOL BANDS W/G8084-12 UR 26

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011882026220·dentaform® Band, Tooth 16, Size 26/Roth 22

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011882026180·dentaform® Band, Tooth 16, Size 26/Roth 18

    dentaform®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011882026000·dentaform® Band, Tooth 16, Size 26

    K-MED SILICONE SUMP DRAIN

    FDA 510(k)

    FLAT SILICONE DRAIN

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

    PROMUS PREMIER?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 18, 2014

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·December 20, 2012

    ENDOGIA 35 STAPLER

    FDA Adverse Event
    ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 28, 2010

    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