BEUDAMED
    11 results · 17ms · 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.

    CHICK III SURGICAL LIGHTING SYSTEM

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

    Map-iT

    FDA UDI
    ACCESS POINT TECHNOLOGIES, INC.·00818083015398·Fixed, 10 electrode, MPA, 5-5-5-24-4-4-4-4-4mm ...

    Vu a-POD Prime NanoMetalene

    FDA UDI
    Seaspine Orthopedics Corporation·10889981126865·Prime NM Implant, 39x30mm x 18mm, 30 Deg

    ORTHOMED

    FDA UDI
    ORTHO-MED, INC.·B8039018300·MEDIAL MALLEOLAR/SMALL BONE FRAGMENT CLAMP

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 4, 2024

    ANSER Clavicle Pin

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ZMACHINE, MODEL DT-100

    FDA 510(k)
    FDA Class 2 ·Neurology

    ES2

    FDA Adverse Event
    Malfunction ·STRYKER SPINE·Product code NKB·June 24, 2014

    TOTAL ASR FEM IMP SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·January 8, 2013

    LOW PROFILE SELF-TAPPING BONE SCREW 6.5MM X 20MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·November 17, 2010

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 4, 2024