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 ×

    ABLATE-IQ

    FDA 510(k)
    FDA Class 2 ·Radiology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694036849·FPS 2.0mm Angled Locking/Compression Guide

    LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DUREX FLAVORED LATEX CONDOM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    AVAULTA PLUS POSTERIOR

    FDA Adverse Event
    Injury ·BARD PHARMACEUTICALS·Product code FTL·November 13, 2008

    MEDTRONIC SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LKK·August 25, 2011

    PELVICOL ACELLULAR COLLAGEN MATRIX 4X7CM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·July 8, 2013

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·January 11, 2018

    CLS SPOTORNO, STEM, 125, UNCEMENTED, 9.0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·August 28, 2018

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025