BEUDAMED
    105 results · 34ms · 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.

    MUELLER HINTON

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006015·FOUNDATION LATERAL CAGE - 18MM X 60MM X 15MM, ...

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006008·FOUNDATION LATERAL CAGE - 18MM X 60MM X 8MM, 0...

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006011·FOUNDATION LATERAL CAGE - 18MM X 60MM X 11MM, ...

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006010·FOUNDATION LATERAL CAGE - 18MM X 60MM X 10MM, ...

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006009·FOUNDATION LATERAL CAGE - 18MM X 60MM X 9MM, 0...

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006013·FOUNDATION LATERAL CAGE - 18MM X 60MM X 13MM, ...

    FOUNDATION System

    FDA UDI
    CORELINK LLC·M72583006012·FOUNDATION LATERAL CAGE - 18MM X 60MM X 12MM, ...

    NeoGen

    FDA UDI
    ENERGIST LIMITED·05060440520266·NeoGen 25mm 3x Nozzle (Grey)

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955932175·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955929977·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955931079·Percutaneous Transluminal Angioplasty Balloon C...

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127020766·Full Hemisphere Reamer Size 60

    SPINEMED

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Light Based Hair Removal Device GP592

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

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK AND AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (AICD) SYSTEMS

    INTELLIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·January 21, 2025

    HERO GRAFT

    FDA Adverse Event
    Injury ·HEMOSPHERE, INC.·Product code DSY·May 23, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 13, 2012

    AVALON ELITE

    FDA Adverse Event
    AVALON LABORATORIES, LLC·Product code DWF·September 9, 2010