Healthcare Industry News:  CerOx 

Devices Monitoring Neurology FDA

 News Release - February 7, 2011

Ornim, Inc. Announces FDA Clearance for Non-Invasive Brain Oximetry and Blood Flow Monitoring

SANTA CLARITA, Calif.--(Healthcare Sales & Marketing Network)-- Ornim, Inc. is pleased to announce the receipt of 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the CerOx 3210F monitor. Additionally to its previous clearance for non-invasive monitoring of regional hemoglobin oxygen saturation in the brain or skeletal muscle, the CerOx 3210F is now also intended for use as a non-invasive monitor of blood flow in tissue of adults.

The CerOx 3210F is currently the only device to use a single, non-invasive probe for simultaneously and independently measuring both oximetry and blood flow parameters, together providing a clear indication of tissue perfusion. The flow adds an important dimension in monitoring the tissue, helping personalize patient treatment while potentially decreasing the overall costs associated with factors such as length of hospitalization and stay in intensive care.

A non-invasive device that can provide both oximetry and flow data will bring neuromonitoring to a new level. These parameters will enable the intensivist to optimize the physiologic variables for an individual patient, at a particular time, and guide management, noted Dr. Daryl Gress of the University of Virginia Health System in Charlottesville, VA.

We are very pleased with the FDAs decision. Ornim is now able to market the only non-invasive monitor displaying both oximetry and flowmetry information. With over 20% annual growth in the oximetry monitoring market alone, the clinical demand is clear. Moreover, the clinical community is sending us clear signals that the added dimension of flow/perfusion may make a real difference in patient care. We are determined to respond to that by bringing CerOx to the market quickly and efficiently, stated Yitzhak Zilberman, CEO of Ornim, Inc.

About Ornim, Inc.

Ornim, Inc. is dedicated to providing physicians with the most advanced monitoring tools to direct safe and decisive patient care when the perfusion of vital tissue is at stake. The company is headquartered in Santa Clarita, California with a research and development subsidiary (Or-Nim Medical Ltd) in Lod, Israel. The company was founded in 2004 and is covered by a broad Intellectual Property (IP) portfolio worldwide.

For more information, please visit www.ornim.com or contact Kevin Lev, Marketing Director, at +972 (54) 447-2610.


Source: Ornim

Issuer of this News Release is solely responsible for its content.
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