BEUDAMED
    783 results · 32ms · 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 ×

    V.A.C. DERMATAC Drape

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

    VHS VARI-ANGLE HIP SCREW

    FDA UDI
    Biomet Orthopedics, LLC·00880304279452·

    Olympus

    FDA UDI
    Gyrus ACMI, LLC·00821925046283·nCare 4K Accessories

    Accufit

    FDA UDI
    Ortho Organizers, Inc.·00190707183653·Accufit Molar Bands Lower Left First Molar 39

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031561·1.6mm Short CA Driver Stem, Dental Latch

    Quala

    FDA UDI
    NATIONAL DISTRIBUTION & CONTRACTING, INC.·D0232003901·Quala X-ray Cover 15 X 26

    VITAL SHIELD GOLD POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODIFICATION TO FETAL ASSIST

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

    MPACT ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 31, 2025

    DIRECT DRIVE LCA

    FDA Adverse Event
    Other ·APPLIED MEDICAL RESOURCES·Product code GDO·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·July 1, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    MPACT EXTENSION

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·April 2, 2026

    MPACT ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 18, 2025

    MECTACER BIOLOX DELTA FEMORAL BALL HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 19, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021