BEUDAMED
    32 results · 24ms · 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 ×

    CORTEX METAMAX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00163011·

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001631·artVeneer life upper anteriors, BL, BL4

    Scanlan® SURG-I-BAND® color coding

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159001280·Scanlan® SURG-I-BAND® color coding - Narrow, Ye...

    NA

    FDA UDI
    aap Implantate AG·04042409048067·K-wire with trocar point, ø1.6, L 310

    3D HDRAULIC FINE MICROMANIPULATOR MO-188NE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    URANUS, COMFORTOUCH LASER SYSTEM

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

    OMYRA MESH (BRANDED AS MOTIFMESH IN THE US)

    FDA Adverse Event
    Other ·PROXY BIOMEDICAL LTD.·Product code FTL·November 20, 2012

    CLS SPORTORNO STEM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·April 3, 2020

    FLAT HUBLESS SILICONE DRAIN

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, INC.·Product code GCY·March 8, 2013

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 25, 2011

    PRECISION XTRA/ OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·February 7, 2008

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·July 9, 2018

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 22, 2012

    STEM EXTENSION STRAIGHT SPLINED UNCEMENTED 12 MM DIAMETER +135 MM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 14, 2021

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 7, 2021

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 7, 2021

    "2.4MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·March 30, 2018

    TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·March 30, 2018

    TMJ SYSTEM RIGHT STANDARD MANDIBULAR COMPONENT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·March 30, 2018