BEUDAMED
    8 results · 19ms · 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.

    EDWARDS-WALLACE BOURNE HALL CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756364157·THYROID/ NECK PACK PGYBK

    OSSEOFUSE DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    BODYGEM, MODEL HB211

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC·Product code FNL·December 3, 2012

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 19, 2010

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·July 2, 2014

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021