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    Farapulse Inc

    Manufacturer
    🇺🇸 United States·2 Importers

    FARAPULSE, INC.

    FDA registration
    FARAPULSE, INC.·1 product·🇺🇸 United States

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·December 16, 2022

    PENTARAY NAV

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code MTD·May 30, 2025

    FARAPULSE PULSED FIELD ABLATION SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·February 28, 2025

    CARTO

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER·Product code DQK·October 20, 2025

    INQUIRE

    FDA Adverse Event
    Injury ·MERIT MEDICAL SYSTEMS INC·Product code DQX·August 28, 2024

    FARAPULSE PULSED FIELD ABLATION SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·July 24, 2024

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·June 11, 2024

    FARAPULSE CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·January 20, 2026

    VERSACROSS STEERABLE SHEATH

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC. / BAYLIS MEDICAL COMPANY, INC.·Product code DYB·March 17, 2025

    PULSED FIELD ABLATION (PFA) SYSTEM /ABLATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code QZI·July 28, 2025

    THERMOCOOL SF NAV

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·May 9, 2025

    PERCLOSE VASCULAR SUTURE DELIVERY DEVICE

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code MGB·May 8, 2025

    FARAWAVE PULSED FIELD ABLAT ION CATHETER, 31MM

    FDA Adverse Event
    Malfunction ·FARAPULSE, INC.·Product code QZI·July 18, 2024

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·FARAPULSE, INC.·Product code DRA·August 2, 2024

    FARAWAVE PULSED FIELD ABLATION CATHETER, 31MM

    FDA Adverse Event
    Injury ·FARAPULSE, INC.·Product code QZI·August 6, 2024

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·FARAPULSE, INC.·Product code DRA·July 23, 2024

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·FARAPULSE, INC.·Product code DRA·September 11, 2024

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·FARAPULSE, INC.·Product code DRA·August 12, 2024