BEUDAMED
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    LimFlow Inc.

    FDA registration
    LimFlow Inc.·4 products·🇺🇸 United States

    LIMFLOW ARC

    FDA Adverse Event
    Malfunction ·LIMFLOW INC.·Product code PDU·July 12, 2024

    LIMFLOW EXTENSION STENT GRAFT

    FDA Adverse Event
    Injury ·LIMFLOW INC.·Product code QWN·October 17, 2025

    LIMFLOW VECTOR

    FDA Adverse Event
    Malfunction ·LIMFLOW INC.·Product code MGZ·October 15, 2025

    LIMFLOW TRANSFORMING CLTI ARC

    FDA Adverse Event
    Injury ·LIMFLOW INC.·Product code PDU·June 28, 2024

    LIMFLOW V-CEIVER

    FDA Adverse Event
    Malfunction ·LIMFLOW INC·Product code MMX·November 19, 2024

    LIMFFLOW STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·LIMFLOW INC·Product code QWN·March 26, 2025

    LIMFLOW ARC

    FDA Adverse Event
    Malfunction ·LIMFLOW INC·Product code PDU·March 14, 2025

    LIMFLOW ARC

    FDA Adverse Event
    Malfunction ·LIMFLOW INC·Product code PDU·January 22, 2025

    Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23

    FDA Recall
    Open, Classified ·LimFlow, Inc.·Product code MGZ·December 5, 2025

    Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23

    FDA Enforcement
    Class II ·Ongoing·LimFlow, Inc.·February 4, 2026