BEUDAMED
    10 results · 37ms · 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 ×

    Aimanfun Lumea Comfort, A-2789/A-3588

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

    TOTAL IPOLY XE 29MM X 7MM CEMENTED OVAL PATELLA IMPLANT

    FDA UDI
    Conformis, Inc.·M572POV0212907011·

    LIQUISPX LIQUID SALIVA OR UNRINE DRUG OF ABUSE CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    CONFIDENCE HIGH VISCOSITY SPINAL CEMENT, 16G / 20G

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FG 6301 DUAL CHNL VOL INF PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·October 29, 2008

    KENTROX SL 65/16 STEROID

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·July 12, 2011

    MONOCRYL PLUS SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·July 9, 2013

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025