BEUDAMED
    7 results · 18ms · 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.

    150 DRIVER REAMER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ERA® Implant Abutment Micro 0°, 6mm Cuff (AX)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549103865·Implant retained overdentures are an establishe...

    DEVILBISS SLEEP RECORDER MODEL # RM60

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARTHREX FRACTURE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 15, 2014

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 31, 2012

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code KNS·August 12, 2010