SonarMed Receives FDA Clearance for Real-time Monitoring Device for Endotracheal Tubes in Pediatric Patients

January 27, 2016

Carmel, Indiana, February 1, 2016 SonarMed announced today that they received FDA 510(k) clearance for their AirWave Monitoring System for neonatal (newborn) and pediatric patients, a new device that provides real-time monitoring of the endotracheal tube, a tube inserted into the windpipe to aid in breathing. The SonarMed AirWave system pioneered the use of acoustic reflectometry to continuously monitor the endotracheal tube for movement and obstruction.

The device pinpoints the exact location of the tip of the tube immediately identifying any obstructions or placement issues. Tubes often move, causing them to come out or go deeper into the lungs, which can cause complications. This technology may allow clinicians to take action before a serious or potentially life-threatening problem occurs.

Each year, as many as 36 percent of patients on life support endure complications related to the poor placement of or obstruction in breathing tubes. When complications occur with premature babies, 31 percent of those suffer serious harm. Locating and positioning the tube in infants can be extremely challenging and complications are dangerous and costly. A recent clinical study indicated that when a breathing tube comes out unexpectedly in pediatric patients the cost can be over $36,000 per incident.

“Until now, neonatologists have not had a single tool to allow for the detection of blocked, malpositioned or completely dislodged endotracheal tubes, all of which are known to significantly increase both long-term morbidity and mortality. The engineers of SonarMed have applied safe, proven technology to solve all these problems in our smallest, most critical patients through the use of a single unique device,” said Dr. Jamie W. Powers, medical director, Neonatal Intensive Care Unit, Pediatrix Medical Group, Huntington Memorial Hospital.

In fact, more than 90 percent of physicians surveyed stated that they are dissatisfied with the current methods for identifying obstructions and misplaced tubes.

SonarMed will market the pediatric device to a very select group of top-tier hospitals in the next six months.

Jim Tyree, executive chairman of SonarMed and former president of Abbott Biotech Ventures, praised the SonarMed team. “This is an outstanding accomplishment for the team and while the most urgent need for this device is in the NICU, this very well could become standard of care in all ICUs and operating rooms”, he said.

About SonarMed

SonarMed, Inc. is privately held medical device company in Carmel, Indiana that specializes in developing solutions that increase patient safety while significantly decreasing healthcare costs. SonarMed is dedicated to reducing the dangerous challenges around airway management in pediatric and adult critical care settings. SonarMed has focused their expertise on researching and developing innovative airway monitoring products that will potentially satisfy a 350 million dollar market within NICU and pediatric facilities, part of an overall 1 billion dollar market. The Airwave System is currently 510(k) cleared and CE marked for use in adult and neonate patients and will be introduced to select hospitals in first quarter 2016.

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