BEUDAMED
    6 results · 22ms · 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.

    NEW-STIM SPINAL ADJUSTMENT INSTRUMENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    QUALTEX MAGNETIC INSTRUMENT DRAPE

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

    BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ECHO POROUS FEMORAL RED NC 10X130 STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 5, 2013

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code MTA·December 21, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 18, 2014