BEUDAMED
    43 results · 21ms · Sources: EU EUDAMED, US FDA

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    XENMATRIX SURGICAL GRAFT

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

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481120855·LOCATOR R-Tx Abutment For UF(II) Narrow Platfor...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319740699·Jones Towel Clamp 2-1/4" (5.6cm), lightweight

    n/a

    FDA UDI
    Ortho Development Corporation·00822409067091·Stem Extension Trial Diameter 14x50mm

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981440848·Drill Guide Sleeve

    MULTIFUNCTIONAL LINEAR PEN

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

    DBX DEMINERALIZED BONE MATRIX PUTTY, PASTE AND MIX

    FDA 510(k)
    FDA Class 2 ·Dental

    MICROFRANCE® INSTRUMENT

    FDA Adverse Event
    Malfunction ·XOMED MICROFRANCE MFG·Product code GEI·January 23, 2015

    VIZIGO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·October 24, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2025

    GEM V/NV 20D 1CV 2SS DEHP FREE

    FDA Adverse Event
    Malfunction ·Product code FPA·August 17, 2021

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014

    HAKIM INLINE PROGRAMMABLE VALVE SG

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·May 31, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 27, 2011

    ENDOSKELETON¿ TT INTERBODY SYSTEM

    FDA Adverse Event
    Malfunction ·TITAN SPINE, A DIVISION OF MEDTRONIC·Product code HWR·December 1, 2025

    CLEARLINK DUO-VENT SOLUTION ADMINISTRATION SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·December 30, 2021

    ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTQ·September 6, 2024

    UNKNOWN

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 5, 2022

    KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 / Infant Silicone King LAD¿ Patient Size: 10-20kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·February 12, 2026