BEUDAMED
    32 results · 23ms · 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 ×

    Silhouette Instalift

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

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180107939·KAHN UTERINE TRIGGER CANNULA, 25CM (10") W/3 SP...

    GERALD TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084537·GERALD TISSUE FORCEPS TUNGSTEN CARBIDE DUST TIP

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006231·Drill Guide, Neutral, Short Pointed Cannula

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2522001400·Straight Titanium Rod

    CorticaLINK MI

    FDA UDI
    LINKSPINE, INC.·00817329023166·5.0mm Cobalt Chrome Rod: 140mm Curved

    SURE LIFE

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC.·Product code DXN·June 7, 2018

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555252200140·Taurus Pedicle Screw System- Straight Rod 5.5x1...

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102200140·Straight Rod 6.0mm, 140mm

    CLINI-DENT

    FDA 510(k)
    FDA Class 1 ·Dental

    VOXAR'S CALCIUM SCORING PRODUCT

    FDA 510(k)
    FDA Class 2 ·Radiology

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 6, 2002

    FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 5, 2003

    ALINITY C PROCESSING MODULE

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·March 20, 2025

    REVERSE #SHORT HUM. BODY 140°

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code MBF·November 11, 2022

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 10, 2016

    OMRON 5 SERIES UPPER ARM BLOOD PRESSURE MONITOR

    FDA Adverse Event
    Injury ·OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.·Product code DXN·May 27, 2021

    THE CLOSER AK

    FDA Adverse Event
    Injury ·PERCLOSE, INC.·Product code MGB·July 6, 2004

    NANOKNIFE SYSTEM

    FDA Adverse Event
    Injury ·ANGIODYNAMICS, INC.·Product code GEI·July 31, 2012

    COLLEAGUE PRE-P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011