BEUDAMED
    9 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 ×

    TEMPOFIT, MODEL 02693

    FDA 510(k)
    FDA Class 2 ·Dental

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517803528·ALBINS Cobb, 12mm Bayoneted Superior

    NANOHYBRID COMPULES 15-.3 Gm (C2)

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77819940121·Nanohybrid Composite contains a new ytterbium f...

    MINICLINIC PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CAPNOSTREAM20 WITH MICROMEDICO2 MODULE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    2.0 MM TI MATRIXMANDIBLE SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA) MONUMENT·Product code JEY·February 27, 2013

    ETS-FLEX - ENDOSCOPIC

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 16, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·August 8, 2014

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026