BEUDAMED
    14 results · 20ms · 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.

    MatriDerm pluS+ Bi-Layer

    FDA 510(k)
    FDA Unclassified ·Unknown

    Darby Dental Supply, LLC

    FDA UDI
    DARBY DENTAL SUPPLY, LLC·00889813036013·C-FILE 21MM #10

    GIBSON HEALTHCARE

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975012401·Gibson Healthcare Membrane 3-4 Regenertive Coll...

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·April 20, 2026

    5MP Color LCD Monitors C53S+, C53SP+, 5MP Monochrome LCD Monitors G53S+, G53SP+

    FDA 510(k)
    FDA Class 2 ·Radiology

    PARALLAX ACRYLIC RESIN WITH TRACERS TA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·May 1, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    BD POSIFLUSH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code NGT·March 20, 2026

    POSIFLUSH

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FOZ·April 6, 2026

    ENDOPLEGE SINUS CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DWF·November 26, 2008

    OXFORD UNICOMPARTMENTAL KNEE FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code HRY·September 2, 2011

    1722028-2013-01307

    FDA Adverse Event
    Malfunction ·GAMBRO BCT, INC.·July 29, 2013

    LOGIC CR TIB INSERT SLOPE++, SZ 2, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·November 28, 2022