BEUDAMED
    22 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HySil Plus Impression Materials

    FDA 510(k)
    FDA Class 2 ·Dental

    M-TWO INSTRUMENT

    FDA UDI
    SWEDEN & MARTINA SPA·D7700457543·M-TWO INSTRUMENT 10/.04 21 MM, 6 PCS

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777433·LUMBAMED PLUS FLEX PAD WM SILVER I

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100410·Caddie Lid, Curved Rods

    EXPLOR

    FDA UDI
    Biomet Orthopedics, LLC·00880304438323·

    Salvo® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642174434·8.5 x 80 mm Bone Screw, Cannulated, 3 mm Pitch

    SLT DIFFUSER FIBER

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

    FlexPointer 1.5 Single Use, FlexTube 3 Single Use

    FDA 510(k)
    FDA Class 2 ·Neurology

    CONMED PENCIL

    FDA Adverse Event
    Other ·CONMED ELECTROSURGERY·Product code GEI·February 5, 2003

    EXPLOR 7X26MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·Product code KWI·July 20, 2021

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·October 21, 2008

    ENDO STITCH 10MM SUTURING DEVICE

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code KOG·August 3, 2011

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 8, 2013

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·August 1, 2025

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·August 1, 2025

    EXPLOR MODULAR RADIAL STEM WITH SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·June 28, 2017

    EXPLOR 8X28MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·August 1, 2025

    EXPLOR 8X28MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·August 1, 2025

    EXPLOR 8X28MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·February 5, 2024

    EXPLOR 12X24 MM IMPLANT HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·July 2, 2024