BEUDAMED
    7 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    CONDYLAR PROSTHESIS OF MANDIBLE W/HEAD

    FDA 510(k)
    FDA Class 2 ·Dental

    MTA2.1 MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    M3290A INTELLIVUE INFORMATION CENTER SOFTWARE RELEASE E.01 AND INTELLIVUE CLINICAL NETWORK ON VLAN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    2.8MM THREADED GUIDE WIRE- TROCAR POINT 300MM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXT·June 20, 2019

    LIGAMAX CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·May 30, 2014

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·November 20, 2012

    PATIENT ROOM WALL SAVER RECLINER

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code FRK·September 10, 2010