BEUDAMED
    10 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.

    JAW SPREADER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    OMNI Knee

    FDA UDI
    Omni Life Science, Inc.·00841690101734·Ultra Tibial Insert CS, Size 5 x 10mm

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746091285·DB BKT LP V-SLOT LR CEN 022 T-5 A+2 R=0

    SeaSpine Spacer System - Redondo™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981044992·Redondo Trial 30mm x 24mm x 10mm, 12 Deg

    CARDIO REP CK ISOENZYME KIT - 3310

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SIA THYROID STIMULATING HORMONE ELISA KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PANOSCREEN I, II, III

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·June 15, 2011

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 10, 2010

    S3 EX - 3005

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 30, 2013

    COYOTE? ES

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·July 15, 2014