BEUDAMED
    14 results · 28ms · 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 ×

    Profound Matrix

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

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776390488·Bruns Curette, 8", straight, oval, size 00000

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780183709·Integra® Jarit® Bruns Oval Cup Curette, 8", Str...

    NA

    FDA UDI
    SYNTHES (U.S.A.) LP·10886982164797·SCALLOPED DISTAL TIBIA PLATE 10 HOLES

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361023364·Ø8MM FUSION SCREW, GEN II, SACROFUSE, 70MM

    ARTELON SPACER CMC-1

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LUXER SHADED ZIRCONIA

    FDA 510(k)
    FDA Class 2 ·Dental

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024119437·

    Widex

    FDA UDI
    Widex A/S·05706069691986·Widex BEYOND B-F2 (Copper brown ) 440, Telecoil...

    VERSA-DIAL 50X21X57 HUM HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·October 5, 2017

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 24, 2008

    VICTORY XL DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·September 9, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 22, 2013

    LG HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·September 29, 2017