BEUDAMED
    13 results · 24ms · 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 ×

    Knee+

    FDA 510(k)
    FDA Class 2 ·Neurology

    DXTEND HUM BROACH DIA 14 MM

    FDA UDI
    ENZTEC LIMITED·09421038410899·A reusable surgical instrument intended to be u...

    DXTEND HUM BROACH DIA 10 MM

    FDA UDI
    ENZTEC LIMITED·09421038410875·A reusable surgical instrument intended to be u...

    DXTEND HUM BROACH DIA 12 MM

    FDA UDI
    ENZTEC LIMITED·09421038410882·A reusable surgical instrument intended to be u...

    DXTEND HUM BROACH DIA 16 MM

    FDA UDI
    ENZTEC LIMITED·09421038410905·A reusable surgical instrument intended to be u...

    DELTA XTEND

    FDA UDI
    DEPUY (IRELAND)·10603295116509·DELTA Xtend GLENOID CANNULATED STOP DRILL DIA 7...

    LnK MIS Spinal System, PathLoc-L MIS Spinal System, AccelFix-MIS Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMSCO CENTURY STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 20, 2025

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·November 17, 2008

    NEXGEN CR FLEX ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·August 23, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013

    GLENOID CANNULATED STOP DRILL

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HTW·February 25, 2022