BEUDAMED
    340 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 ×

    KOREA OGK CO., LTD.

    FDA registration
    KOREA OGK CO., LTD.·4 products·🇰🇷 South Korea

    TSINGTAO OGK CO.,LTD

    FDA registration
    TSINGTAO OGK CO.,LTD·2 products·🇨🇳 China

    OGK HANOI CO.,LTD

    FDA registration
    OGK HANOI CO.,LTD·2 products·🇻🇳 Vietnam

    CURAPLEX

    FDA Adverse Event
    Malfunction ·BOUND TREE MEDICAL, LLC·Product code OGK·November 21, 2023

    CURAPLEX

    FDA Adverse Event
    Malfunction ·BOUND TREE MEDICAL, LLC·Product code OGK·November 21, 2023

    SMITHS MEDICAL PORTEX LARYNGOTRACHEAL ANESTHESIA KIT

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code OGK·November 15, 2019

    smiths medical portex Tracheal Intubation Stylet, REF 100/120/200, 4.0mm OD X 335mm, 10/box, sterile.

    FDA Recall
    Terminated ·Smiths Medical ASD Inc.·Product code OGK·August 4, 2021

    superDimension Systems AAS00016-xx with Software Version 4.0-4.9. Indicated for use for displaying images of the tracheobronchial tree to aid the physician in guiding endoscopic tools or catheters in the pulmonary tract and to enable marker placement within soft lung tissue. It does not make a diagnosis and is not an endoscopic tool. Not for pediatric use.

    FDA Recall
    Terminated ·superDimension, Inc·Product code OGK·June 18, 2012

    Orotracheal Intubation Guide Kit

    FDA classification
    FDA Class 2 ·Orotracheal Intubation Guide Kit

    OGI, LLC

    FDA registration
    OGI, LLC·3 products·🇺🇸 United States

    OAK RIDGE PRODUCTS

    FDA registration
    OAK RIDGE PRODUCTS·4 products·🇺🇸 United States

    Mighty Oak Medical

    FDA registration
    Mighty Oak Medical·3 products·🇺🇸 United States

    WHITE OAK ORTHODONTIC PRODUCTS

    FDA registration
    WHITE OAK ORTHODONTIC PRODUCTS·22 products·🇺🇸 United States

    POST OAK INNOVATIONS, INC.

    FDA registration
    POST OAK INNOVATIONS, INC.·1 product·🇺🇸 United States

    GoldenDent

    FDA UDI
    GoldenDent·00850011211939·Advanced Grafting Kit (11 Instruments and Casse...

    Guidewire Kit

    FDA UDI
    CURVAFIX, INC.·10855068008119·A single use kit, composed of a sterile package...

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756868747·CARE GIVER KEY

    LAP CHOLE KIT 2 GK

    FDA UDI
    APPLIED MEDICAL RESOURCES CORPORATION·20607915120843·Kit Contains: CA090, DIRECT DRIVE LCA 3/BX C0R4...

    LAP CHOLE KIT 4 GK

    FDA UDI
    APPLIED MEDICAL RESOURCES CORPORATION·20607915120867·Kit Contains: CA090, DIRECT DRIVE LCA 3/BX C0R4...

    LAP CHOLE KIT 7 GK

    FDA UDI
    APPLIED MEDICAL RESOURCES CORPORATION·20607915120881·Kit Contains: CA090, DIRECT DRIVE LCA 3/BX CTR3...