BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LASER HAIR GROWTH CAP

    FDA Adverse Event
    Injury ·UNKNOWN·Product code OAP·February 26, 2025

    MILLENIUM ANTI-SNORING DEVICE

    FDA 510(k)
    FDA Class 2 ·Dental

    ULTRADENT CITRIC ACID 10% SOLUTION

    FDA 510(k)
    FDA Unclassified ·Unknown

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    HOMECHOICE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 17, 2011

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CTR.·Product code HQC·August 22, 2008

    Tapered Screw-Vent Implant, MTX, 4.7mm x 11.5mm, 4.5mm Platform. Catalog Number TSVWB11, Lot 62470008. Class II, 510(k) K13227.

    FDA Enforcement
    Class II ·Terminated·Zimmer Dental Inc·February 5, 2014

    Tapered Screw-Vent Implant, MTX, 4.7mm x 11.5mm, 4.5mm Platform. Catalog Number TSVWB11, Lot 62470008. Class II, 510(k) K13227.

    FDA Recall
    Terminated ·Zimmer Dental Inc·Product code DZE·January 6, 2014