BEUDAMED
    10 results · 28ms · 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 ×

    SPECTACLE FRAMES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NA

    FDA UDI
    Richard Wolf GmbH·04055207044810·SELF-RETAINING SLEEVE 12.1MM WL 35MM for smoot...

    Nu-Edge Cobalt Chromium Brackets

    FDA UDI
    TP ORTHODONTICS INC·00192029046203·LL BI W/HK

    SeaSpine Spacer System - Hollywood

    FDA UDI
    Seaspine Orthopedics Corporation·10889981090067·Straight Chisel, Wide

    THROMBOLYTIC ACTIVITY TEST

    FDA 510(k)
    FDA Class 2 ·Hematology

    DU PONT DIMENSION(R) SALICYLATE(SAL) METHOD

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 27, 2014

    ADVANCE(R) II COCR TIBIAL BASE

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HRY·December 21, 2010

    GENESIS

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 7, 2013

    Alcon Custom Pak

    FDA Enforcement
    Class II ·Ongoing·Alcon Research, LTD.·August 23, 2023