BEUDAMED
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    FFX Inc.

    FDA registration
    FFX Inc.·1 product·🇺🇸 United States

    FFF IMPORT INC

    FDA registration
    FFF IMPORT INC·1 product·🇺🇸 United States

    FLEX 10

    FDA Adverse Event
    Injury ·AFX INC.·Product code NEY·January 26, 2004

    FLEX 4

    FDA Adverse Event
    Injury ·AFX INC.·Product code NEY·March 16, 2002

    FLEX 10

    FDA Adverse Event
    Injury ·AFX INC.·Product code NEY·March 24, 2003

    AFX

    FDA Adverse Event
    Malfunction ·AFX INC·Product code NEY·July 20, 2002

    AFX FLEX 10

    FDA Adverse Event
    Injury ·AFX INC.·Product code NEY·April 3, 2003

    AFX FLEX 10

    FDA Adverse Event
    Malfunction ·AFX INC.·Product code NEY·April 3, 2003

    ATMOSCLEAN

    FDA Adverse Event
    Malfunction ·MASTER FX, INC.·Product code LRJ·July 22, 2020

    Drainer(R) Centesis Catheters: (a) REF 8810, 5F x 9cm (b) REF 8811, 6F x 9cm (c) REF 8812, 5F x 15cm Product The Drainer centesis catheter is intended for use in percutaneous fluid aspirations and small volume drainage procedures.

    FDA Enforcement
    Class II ·Terminated·Vascular Solutions, Inc.·June 27, 2018

    SILVERHAWK XLV - REFORM

    FDA Adverse Event
    FOX HOLLOW TECHNOLOGIES, INC.·Product code MCW·January 27, 2004

    REFORM (SILVERHAWK) PERIPHERAL CATHETER

    FDA Adverse Event
    Other ·FOX HOLLOW TECH. INC.·Product code MCX·October 7, 2003

    REFORM (SILVERHAWK) PERIPHERAL CATHETER

    FDA Adverse Event
    Other ·FOX HOLLOW TECHNOLOGIES, INC.·Product code MCX·October 13, 2003

    SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Malfunction ·FOX HOLLOW TECHNOLOGIES, INC.·Product code MCW·May 24, 2007

    REFORM/SILVERHAWK CATHETER SYSTEM

    FDA Adverse Event
    Other ·FOX HOLLOW TECHNOLOGIES INC.·Product code MCX·September 2, 2004

    SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Other ·FOX HOLLOW TECHNOLOGIES, INC.·Product code MCW·February 15, 2007

    SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Other ·FOX HOLLOW TECHNOLOGIES, INC.·Product code MCW·March 9, 2007

    REFORM/SILVER HAWK CATHETER

    FDA Adverse Event
    Other ·FOX HOLLOW TECHNOLOGIES INC.·Product code MCW·September 23, 2004

    SILVERHAWK

    FDA Adverse Event
    Malfunction ·FOX HOLLOW TECHNOLOGIES, INC.·Product code MCW·January 12, 2006

    SILVERHAWK PERIPHEREAL PLAQUE EXCISION SYSTEM

    FDA Adverse Event
    Malfunction ·FOX HOLLOW TECHNOLOGIES, INC.,·Product code MCW·November 22, 2006