BEUDAMED
    11 results · 21ms · 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 ×

    TRUMATCH Personalized Solutions

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169599420·TRIAL 2193540 O25 IB 27MM 18 DEG 16X40

    AGXO

    FDA UDI
    Oticon A/S·05707131343369·G100, MINIRITE T 312 2.4G C093 AGXO

    PSORIA-LIGHT

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

    RELIANCE LUMBAR IBF SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD SYRINGE 5ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·January 15, 2026

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 5, 2011

    KIMVENT ORAL CARE SWAB

    FDA Adverse Event
    KIMBERLY-CLARK HEALTH CARE·Product code KXF·June 27, 2013

    STRATOS

    FDA Adverse Event
    Injury ·MEDXPERT GMBH·Product code HRS·September 11, 2014

    BD SYRINGE 10ML LL BN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·January 15, 2026

    BD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·January 15, 2026