BEUDAMED
    16 results · 17ms · 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.

    EFTEKHAR RECHANNELIZATION DRILL GUIDE

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867125858·HEADLESS COMPRES SCRW 4.3X14MM

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140125·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140162·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140122·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140145·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140165·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140185·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140182·Rotary diamond instruments

    Sunshine Diamonds

    FDA UDI
    Dr. Hopf GmbH & Co. KG·ESUN8643140142·Rotary diamond instruments

    FANA 60

    FDA 510(k)
    FDA Class 2 ·Immunology

    CAMPY 5

    FDA 510(k)
    FDA Class 1 ·Microbiology

    XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·June 10, 2014

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 7, 2010

    FOUNDATION SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code HSD·December 5, 2012

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021