BEUDAMED
    11 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.

    PRUITT ARTERIAL OCCLUSION CHOLANG. CATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mrk, Ocular

    FDA UDI
    KATENA PRODUCTS, INC.·00841668119884·Dell Astig. Marker, 40, 60, & 80 Deg

    BoneCam

    FDA UDI
    MEDLINE INDUSTRIES, INC.·00818614021102·

    Kinetic Dynamic Anterior Cervical Plate System

    FDA UDI
    Life Spine, Inc.·00190837005047·

    O2-MAX

    FDA UDI
    PULMODYNE INC·00841470102562·

    DL Self-adhesive Electrode

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACU-SINCH REPAIR SYSTEM AND ACUMED SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 15, 2014

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 31, 2012

    SYSTEM 5 RECIPROCATING SAW

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·August 12, 2010

    Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty

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