BEUDAMED
    26 results · 26ms · 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.

    MODIFICATION TO: SATELLITE SPINAL SYSTEM

    FDA 510(k)
    FDA Class 3 ·Unknown

    SATELLITE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code NVR·May 5, 2011

    EASY KIT M

    FDA UDI
    TEKNIMED·03760177042117·

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70604151·Mini-Mono-Brackets Ricketts 'N' .018" 1000 Brac...

    Osseofit™ Porous Tissue Matrix

    FDA UDI
    DSM BIOMEDICAL, INC.·00812337021562·

    Rumor

    FDA UDI
    Ortho Organizers, Inc.·00190707004095·Rumor .022 LL4 -17T 0A 0O

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0604250·Tray, Base, 4.25"

    Rumor

    FDA UDI
    Ortho Organizers, Inc.·00190707004101·Rumor .022 LL4 HK -17T 0A 0O

    ISODAN

    FDA 510(k)
    FDA Class 2 ·Dental

    OIS-2500 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·December 1, 2006

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·April 26, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·March 23, 2007

    RESTORE ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 29, 2013

    SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·November 19, 2015

    RESTORE ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 20, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·February 2, 2007

    CORMET RESURFACING

    FDA Adverse Event
    CORIN LTD.·Product code NXT·April 11, 2013

    ADVIA CENTAUR

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JJE·April 16, 2011

    GORE INTRODUCER SHEATH WITH SILICONE PINCH VALVE

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·June 12, 2008