BEUDAMED
    31 results · 21ms · 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 ×

    CAREMATE SPHYGMOMANOMETER WITH STETHOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690196495·AK3 Distal Cutting Block

    CSTAT, MODELS 09-0014-01 AND 09-0014-02

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    neoWave C

    FDA UDI
    XENIX MEDICAL LLC·00818345023840·Cervical Inserter Draw Rod

    icotec Pedicle System 6.0, Rod, Ti, Straight, Ø 6.0 r000 x 140 mm

    FDA UDI
    icotec AG·07640164848563·icotec Pedicle System 6.0, Rod, Ti, Straight, Ø...

    InTess C Cervical Cage System

    FDA UDI
    Kalitec Direct LLC·B07309K0100140·Caddie, Large Implants and Instruments

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014

    BARCOMED 5MP1H

    FDA 510(k)
    FDA Class 2 ·Radiology

    INSTANT-VIEW METHADONE URINE DIP STRIP TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962106167·ø1.4mm K-WIRE, 9", SINGLE DIAMOND (ROUND END), ...

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00812171026600·ø1.4mm K-WIRE, 9", DOUBLE END TROCAR, SMOOTH

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68120190900140·14mm LG Lordotic Expanding Trial, HiJAK™ Cervical

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962106150·ø1.4mm K-WIRE, 9", DOUBLE END DIAMOND, SMOOTH

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900140·14mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962105610·ø1.4mm K-WIRE, 9", SINGLE TROCAR (ROUND END), S...

    COPPERHEAD CERVICAL INTERBODY CAGE

    FDA Adverse Event
    Injury ·EMINENT SPINE·Product code ODP·January 8, 2016

    TGS UKA SYSTEM

    FDA Adverse Event
    Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013

    TGS UKA KNEE SYSTEM

    FDA Adverse Event
    Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013

    TGS UKA SYSTEM

    FDA Adverse Event
    Injury ·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 20, 2014