BEUDAMED
    273 results · 24ms · 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 ×

    AERONEB PROFESSIONAL NEBULIZER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108699661·Implant Insertion Key NP + Conical, Narrow, Long

    SOFT K. AND SOFT K. TORIC (XYLOFICON A) SOFT (HYDROPHILLIC) KERATOCONUS CONTACT LENS FOR DAILY WEAR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PLEURX PLEURAL CATHETER AND DRAINAGE KITS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·March 12, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 13, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 11, 2026

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code OTN·April 12, 2013

    ARCHITECT TOTAL B-HCG

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code DHA·April 27, 2011

    LIGACLIP MCA LARGE APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDO·July 1, 2008

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·ZIMVIE US CORP LLC·Product code DZE·May 4, 2026

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·February 13, 2020

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 23, 2018