BEUDAMED
    15 results · 35ms · Sources: EU EUDAMED, US FDA

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    CRUTCH TIPS & GRIPS

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    N/A

    FDA UDI
    TETRA MEDICAL SUPPLY CORP.·00614138123090·LISTER, 1 LG RING, 7-1/2IN

    Cortera

    FDA UDI
    Xtant Medical Holdings, Inc.·00840311233304·Tap, NAV, Solid, 6.5

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345026292·Removal Tool

    TiWAVE L Lumbar Cage System

    FDA UDI
    Kalitec Direct LLC·B07323K0106500·Removal Tool, Implant

    NA

    FDA UDI
    Zimmer, Inc.·00889024273641·

    ZYSTON ARC INTERBODY SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AT HOME DRUG TEST, MODEL 9073 T

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LOCKING SCREW, FULLY THREADED 5X55 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 30, 2010

    LIBERTY CYCLER SET, DUAL PATIENT CONNECT

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·April 30, 2014

    KAPPA 900 SR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·October 31, 2012

    NONE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020