BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    Trident® Tritanium® PST® Acetabular Shells

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Innomed, Inc.

    FDA UDI
    INNOMED, INC.·00840277125545·Cheng Trephine 10mm

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383507172·Gutta Percha Points is used to root canal filin...

    ZAVATION

    FDA UDI
    Zavation LLC·00842166186781·14mm X 26mm 6° Trial

    AVS ANCHOR-C CERVICAL CAGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO:SYNTHES (USA) TITANIUM WIRE

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

    PELVICOL ACELLULAR COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABS.·Product code FTL·April 4, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·June 21, 2011

    AERO LL FIXATION ANCHOR, 50MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code OVD·March 25, 2019

    Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

    FDA Enforcement
    Class II ·Ongoing·Ventana Medical Systems, Inc.·August 28, 2024

    Cobe CML Duo Flat Sheet Membrane Oxygenator, sterile, (Custom Heart/Lung Packs), Catalog numbers: 067100001, 078002103, 078005802, 078159025, 078201013, 078212009, 078310006, 078332022, 078348014, 078428010, 078688007, 078869003. COBE Cardiovascular, Inc..

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code DTZ·June 26, 2006