Fist Assist Devices
Manufacturing · California, United States · 11-50 Employees
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Overview
Headquarters
PO Box 4015, Los Altos, California, 9402...Phone Number
(833) 434-5283Website
www.fistassistdevices.comRevenue
<$5 MillionIndustry
About Fist Assist Devices
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Fist Assist Devices Tech Stack
A closer look at the technologies used by Fist Assist Devices
Fist Assist Devices News & Media
AIROS Medical and Fist Assist Devices, LLC Announce Launch of Commercial Website for Fist Assist FA-1 Wearable Medical Device
LAS VEGAS--(BUSINESS WIRE)--AIROS Medical and Fist Assist Devices, LLC announce the launch of an e-commerce website for the sale of the Fist Assist FA-1 compression device.Fist Assist Devices Receives FDA “Breakthrough Device” Designation for the World’s First Wearable Vein Dilation Device for ESRD Patients
LAS VEGAS--(BUSINESS WIRE)--Fist Assist Devices, LLC, an innovative medical device company focused on vein dilation to facilitate the Chronic Kidney Disease (CKD) patient’s journey through End-Stage Renal Disease (ESRD), announced today that it received “Breakthrough Device” designation from the U.S. Food and Drug Administration (FDA) for the Fist Assist Model FA-1 device. The FA-1 is the world’s first wearable device for pre-surgical vein dilation that promotes AV fistula creation in adult patFist Assist Devices, LLC Announces Release of the p-FACT Cohort Data
LOS ALTOS HILLS, Calif.--(BUSINESS WIRE)--Fist Assist Devices, LLC, announces that data associated with the p-FACT cohort, a data subset of the recently completed, non-significant risk Fist Assist Clinical Trial (FACT Trial) that focused on vein dilation in stage 4 patients with chronic renal failure, shows clear evidence that the Fist Assist device dilates the perforator vein. The p-FACT data derived from the FACT trial evaluated the use the FA-1 device developed by Fist Assist Devices,Fist Assist Devices, LLC Announces Completion of the Non-Significant Risk FACT Trial
LOS ALTOS HILLS, Calif.--(BUSINESS WIRE)--Fist Assist Devices, LLC, announces completion of the non-significant risk FACT Trial (Fist Assist Clinical Trial). FACT evaluated the use of an intermittent pneumatic compression device, model FA-1, that was developed by Fist Assist Devices, to promote vein dilation in patients with kidney disease, to enable creation of arteriovenous fistulas and to ensure the safety of the device in this patient population. “We are ecstatic to complete FACT and are ve
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Frequently Asked Questions Regarding Fist Assist Devices
Fist Assist specializes in a novel, non-invasive external device designed for vein dilation, particularly to assist in hemodialysis fistula development and phlebotomy procedures. Their primary product, the Fist Assist FA-1, utilizes intermittent pneumatic compression to enhance circulation and facilitate vein preparation for vascular access. Target... Read More