Devices Monitoring FDA

 News Release - January 25, 2021

PEDRA(TM) Technology Receives FDA Breakthrough Device Designation for its PEDRA(TM) Xauron(TM) Real-Time Tissue Perfusion System

Novel perfusion monitor achieves FDA Breakthrough Device Designation for real-time, periprocedural monitoring of tissue perfusion in patients with critical limb threatening ischemia

SINGAPORE, Jan 25, 2021 -- (Healthcare Sales & Marketing Network) -- PEDRA™ Technology, a privately-held company, announced today that the U.S Food and Drug Administration (FDA) has granted the company a Breakthrough Device Designation for the periprocedural use of its PEDRA™ Xauron™ Perfusion System in the treatment of critical limb threatening ischemia (CLTI).

CLTI is a severe form of peripheral artery disease (PAD) that is defined as ischemic rest pain, tissue loss, or gangrene (tissue death) that develops as a result of chronically poor blood flow to the lower limbs. If left untreated, CLTI can lead to limb amputation or death. The 1-year mortality rate of CLTI patients without amputation is 30.3% and with amputation is 40.4%. At 5-years post-CLTI diagnosis, the mortality rate exceeds 50%, which is worse than most cancers.

The Breakthrough Devices Program at the FDA aims to provide patients and providers with timely access to medical devices that provide for more effective treatment and diagnosis of severe diseases, including a prioritized review of market approval regulatory submissions.

"This Breakthrough Device Designation recognizes the compelling need for real-time tissue perfusion monitoring during lower limb revascularization procedures for the treatment of CLTI. To my knowledge, this is the first perfusion monitor for CLTI that has received this designation," said Kareen Looi, CEO of PEDRA Technology. "An improvement in microvascular perfusion at the tissue level is necessary for elimination of rest pain, healing of chronic wounds and for limb salvage. We look forward to developing this important new technology and working closely with the FDA to develop the appropriate clinical program for market approval."

Paul Hayes, MD, vascular surgeon and CMO of PEDRA Technology, commented, "With the Xauron™ device, physicians can at last see real-time perfusion changes during an interventional procedure in the angiographic suite. I'm excited about building on our early clinical data and demonstrating that Xauron™ will save patient lives and limbs."

For additional information about the company and the PEDRA™ Xauron™ Perfusion System, visit PEDRA Technology's website at Pedratech.com.

About PEDRA Technology, Inc.

PEDRA Technology is a medical device company that focuses on the use of tissue perfusion monitoring in the field of peripheral artery disease (PAD) and critical limb ischemia (CLI). The PEDRA™ Xauron™ Perfusion System is not currently approved for sale in the U.S. Learn more at PEDRAtech.com.

Source: PEDRA Technology

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