BEUDAMED
    61 results · 27ms · 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 ×

    LUOFUCON PHMB Alginate Dressing (Rx use), LUOFUCON PHMB Antibacterial Alginate Wound Dressing (OTC use)

    FDA 510(k)
    FDA Unclassified ·Unknown

    NeoFuse HA Enhanced PLIF/TLIF

    FDA UDI
    XENIX MEDICAL LLC·00818345020122·HA CAGE 20L x 10W x 16H

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153158028·MICRO HAEMOST. FORCEPS, H-MOSQ, STR.

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019255·Plate Bender

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193113371·HA PEEK EVOS Straight, ,16mmx8mmx 26mm , FLAT ...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707002987·ARCHES AUSTRALIAN SPECIAL PLUS .016 UP

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021537·A-CIFT SoloFuse 4.2 Screw, Rigid, 16mm

    GE LOGIQ 700

    FDA 510(k)
    FDA Class 2 ·Radiology

    AMX-4 PLUS MOBILE X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MARQUIS VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    ENTRUST AT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    CONCERTO II CRT-D

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NIK·February 15, 2011

    VAPR VUE WIRELESS FOOTSWITCH

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·June 15, 2020

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·February 7, 2012

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·January 17, 2012

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    CIAGLIA BLUE RHINO

    FDA Adverse Event
    Injury ·COOK, COVIDIEN·Product code BTO·October 18, 2010

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 4, 2026

    PALMAZ GENESIS UNKNOWN

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·August 11, 2011

    SAFE-T-CENTESIS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code GCB·May 23, 2013