BEUDAMED
    20 results · 23ms · 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 ×

    Radio Frequency Ablation System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000868154·PLATE 6190052 ANTERIOR CERVICAL 52.5MM

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235916·PLATE 6190052 ANTERIOR CERVICAL 52.5MM

    N/A

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055001·MTM® NO TRACE (TM) 018 UL/4-4

    IN-OVATION® L

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055011·IN-OVATION® L 018 UPPER 6-6

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100520·Caddie, 6.5mm Screws

    IN-OVATION® L

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055101·IN-OVATION® L 018 UL/7-7

    CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/C

    FDA 510(k)
    FDA Class 2 ·Neurology

    CVINSIGHT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONOJECT

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD·Product code PNR·April 14, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

    CARDINAL

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

    STELLARIS ELITE VISION ENHANCEMENT SYSTEM

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQC·March 1, 2022

    25 GA POSTERIOR WIDE-FIELD ELITE PACK

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB, INC·Product code HQC·December 6, 2019

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

    PRODISC-C IMPLANT

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MJO·October 6, 2008

    INTERTAN NAIL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDS·August 4, 2011

    STELLARIS POWER SUPPLY II

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB·Product code HQC·August 1, 2023

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code PNR·April 12, 2024

    RELION INSULIN SYRINGES 1/2ML 31 GAUGE, 8MM (5/16") U-100 100COUNT

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·July 15, 2022