BEUDAMED
    9 results · 29ms · 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 ×

    E-PEN (E-PEN)

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

    PATHWAY ELIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SAFEPICO

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IMPLANT, ENDOSSEOUS, ROOT-FORM

    FDA Adverse Event
    Injury ·J DENTAL CARE SRL·Product code DZE·August 28, 2025

    OPTI-FREE EXPRESS MULTI-PURPOSE DISINFECTING SOLUTION

    FDA Adverse Event
    Injury ·ALCON- FORT WORTH/ALCON LABORTAORIES, INC.·Product code LPN·November 21, 2008

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 12, 2011

    PUSH BUTTON CAP LOADER

    FDA Adverse Event
    Malfunction ·SEASPINE, INC.·Product code NKB·July 18, 2013

    ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026

    Azurion 7 B20; Catalog numbers: (1) 722068, (2) 722226, (3) 722236.

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025