BEUDAMED
    11 results · 20ms · 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 ×

    NeuroStar Advanced Therapy System (Version 3.7)

    FDA 510(k)
    FDA Class 2 ·Neurology

    LessRay

    FDA UDI
    Nuvasive, Inc.·00887517837363·LessRay Assembly Transformer Mount

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707022886·CALIBRA BANDS 2ND MOLAR n.SUL 29

    EZ Bond Universal

    FDA 510(k)
    FDA Class 2 ·Dental

    Auxilock Titanium Interference Screw

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POLARCATH

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQY·November 12, 2008

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·August 31, 2011

    PERMOBIL C400 CORPUS 3G

    FDA Adverse Event
    Injury ·PERMOBIL INC.·Product code ITI·July 11, 2013

    Positron Emission Tomography and Computed Tomography System, Model: uMI 550

    FDA Enforcement
    Class II ·Ongoing·Shanghai United Imaging Healthcare Co., Ltd.·October 19, 2022

    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography (PET) and Computed Tomography (CT), Model uMI 550 Part Number: 88000657 88000057

    FDA Enforcement
    Class II ·Ongoing·Shanghai United Imaging Healthcare Co., Ltd.·April 19, 2023

    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uMI 550 MD, Rx Only

    FDA Enforcement
    Class II ·Ongoing·UIH Technologies LLC·October 29, 2025