BEUDAMED
    84 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 ×

    Ballancer Gold, 1212

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INTERSURGICAL ECOLITE PAEDIATRIC, MEDIUM CONCENTRATION OXYGEN MASK

    FDA UDI
    Intersurgical Incorporated·05030267105083·INTERSURGICAL ECOLITE PAEDIATRIC, MEDIUM CONCEN...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690189794·AK3 Femoral Sizer

    N/A

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055001·MTM® NO TRACE (TM) 018 UL/4-4

    IN-OVATION® L

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055011·IN-OVATION® L 018 UPPER 6-6

    IN-OVATION® L

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055101·IN-OVATION® L 018 UL/7-7

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036032821·

    VITALSENS, AINGEAL, V-POD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VYSIS CLL FISH PROBE KIT (VYSIS LSI TP53 SPECTRUMORANGE/ATM SPECTRUMGREEN) AND LSI D135319 SPECTRUMORANGE/13Q34

    FDA 510(k)
    FDA Class 2 ·Immunology

    SILVERGLIDE

    FDA UDI
    STRYKER CORPORATION·04546540532091·Non-Stick Bipolar Electrosurgical Standard Forc...

    Meduloc Intramedullary Fracture Fixation (IFF) System

    FDA UDI
    MEDULOC, LLC·00810184540458·Removal Trephine (1.5)

    SilverGlide

    FDA UDI
    STRYKER CORPORATION·04546540695888·ProSeries Non-stick Bipolar Electrosurgical For...

    SILVERGLIDE

    FDA UDI
    STRYKER CORPORATION·04546540532244·Non-Stick Bipolar Electrosurgical Precision For...

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·TREO® Abdominal Stent-Graft System

    TREO ABDOMINAL STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·July 12, 2022

    TREO ABDOMINAL STENT-GRAFT SYSTEM

    FDA Adverse Event
    Injury ·BOLTON MEDICAL, INC.·Product code MIH·February 16, 2021

    TREO ABDOMINAL STENT-GRAFT SYSTEM

    FDA Adverse Event
    Injury ·BOLTON MEDICAL, INC.·Product code MIH·May 4, 2022

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·TREO® Abdominal Stent-Graft System

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·TREO Abdominal Stent-Graft System

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·TREO® Abdominal Stent-Graft System