BEUDAMED
    18 results · 21ms · 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 ×

    SAGE Vitrification Kit and SAGE Vitrification Warming Kit

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

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776318628·House Strut Forceps Smooth, Jaw 6.0mm WL 80mm(3...

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169595903·TRIAL 2170560 O25 IB 20MM 0 DEG 16X60

    Bausch + Lomb

    FDA UDI
    Bausch & Lomb Incorporated·00757770430307·FORCEPS STRUT HOUSE

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776410025·House Strut Forceps Smooth, Jaw 6.0mm WL 80mm(3...

    JEDMED

    FDA UDI
    JEDMED INSTRUMENT COMPANY·M633341705600·FORCEPS STRUT HOUSE STRAIGHT

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197452809·McCulloch Blade 6 thor...

    EASY TALK BLOOD GLUCOSE MONITORING SYSTEM MODEL: 6277

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LRTM SURGICAL MESH

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 2, 2025

    MESH, SURGICAL

    FDA Adverse Event
    Injury ·W. L. GORE AND ASSOCIATES, INC.·Product code FTM·August 12, 2023

    COMP RVRS 25MM BSPLT HA+ADPTR R

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 2, 2020

    COMP RVRS SHLDR GLNSP STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 2, 2020

    COMP RVS CNTRL 6.5X25MM ST/RST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·January 2, 2020

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·October 14, 2014

    URETEX SUPPORT PP TRANSOBTUR2 KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·June 12, 2013

    FOX PLUS PTA CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LIT·July 21, 2011

    CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·August 14, 2024