BEUDAMED
    24 results · 22ms · 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 ×

    CONTEC™ Electrocardiograph

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169595996·TRIAL 2171360 O25 IB 20MM 6 DEG 12X60

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111154379·FERGUSON ANGIOTRIBE CVD 6"

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613115739·3K Beaver Style Chuck Round Handle, Collet Uses...

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100776·FLIERINGA FIXATION RING 16MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694045759·PrimaLIF LLIF PEEK Implant, 13mm X 26mm X 60mm,...

    M.U.S.T. MINI POLYAXIAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·August 27, 2025

    MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·April 6, 2018

    MUST MINI POLYAXIAL SCREW 3.5 X 12 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·March 8, 2022

    SHEAUMANN PL-980

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

    OPTICAL GUIDANCE PLATFORM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MUST MINI ROD TI 3.5 X 80MM (STERILE)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 13, 2021

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    MUST MINI MUST MINI POLYAXIAL SCREW 3.5 X 24 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·July 14, 2020

    SIMPLEX P-JAPANESE TWIN PACK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LOD·June 14, 2013

    4C PLUS COULTER CELL CONTROL

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JPK·July 1, 2011

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 17, 2008

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019

    MUST MINI POLYAXIAL SCREW 3.5 X 18 FULL THREAD + NUT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·October 27, 2022

    MUST MINI ROD REDUCTION DEVICE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·September 27, 2019