BEUDAMED
    7 results · 26ms · 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.

    ASSAY SYSTEM, FERRITIN I KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Osstell Beacon

    FDA 510(k)
    FDA Class 1 ·Dental

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·April 30, 2014

    PFC*SIGMA TC3 FEM RT SZ2

    FDA Adverse Event
    Injury ·Product code JWH·October 11, 2012

    RENASYS GO RENTAL

    FDA Adverse Event
    Injury ·Product code OMP·May 19, 2015

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-33, c) 44, 47, 50, 53 head, Large, Item Number 314-13-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-35; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024