BEUDAMED
    11 results · 36ms · Sources: EU EUDAMED, US FDA

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    BIODENTA DENTAL IMPLANT SYSTEM- BONE LEVEL TAPERED

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO DYNALOK CLASSIC SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TANDA MAX

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 31, 2026

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    INTERCHANGEABLE ULNAR ASSEMBLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·October 22, 2019

    HOYER LIFTER

    FDA Adverse Event
    Injury ·BHM MEDICAL INC.·Product code FNG·November 3, 2008

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·September 26, 2014

    INTERCHANGEABLE HUMERAL ASSEMBLY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·October 22, 2019

    Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000

    FDA Enforcement
    Class I ·Ongoing·Covidien·November 8, 2023