Fogarty Innovation Graduate Raydiant Oximetry Raises $5 Million in Oversubscribed Series A2 Financing Round to Support Clinical Study

Fogarty Innovation, a nonprofit educational incubator for medical technology companies, announced today that its graduate, Raydiant Oximetry, Inc., has raised an oversubscribed round of $5 million Series A2 financing. The funding was led by Avestria Ventures, which invests in early-stage women’s health companies, and syndicated by KOFA Healthcare, V-Capital, Band of Angels, FemHealth Ventures, RHIA Ventures and SteelSky Ventures.

Raydiant Oximetry is a clinical-stage medical device company focused on improving women’s and neonatal health. Its innovation is LUMERAHTM, the first-of-its-kind non-invasive fetal oximeter designed to more accurately detect fetal distress during labor and delivery. Current fetal monitoring technology has a low sensitivity that may lead to the failed identification of the distressed baby during labor and delivery, potentially contributing to subsequent newborn birth injury 1. In addition, existing fetal monitoring technology has a low specificity, which can lead to the overuse of emergency C-sections 2.

Initial preclinical results show that LUMERAH significantly improves sensitivity and specificity for the detection of fetal distress and consequently could improve outcomes for both mother and baby during childbirth. Because of its life-improving potential, the FDA has already granted LUMERAH Breakthrough Device status for expedited market approval.

“We are very proud of Neil Ray, MD, founder and CEO of Raydiant Oximetry, and his team for showcasing the opportunity for this type of innovation in the women’s health and neonatal space,” said Andrew Cleeland, CEO of Fogarty Innovation. “Their technology shows potential to have a large impact for millions of mothers and babies around the globe, and is the type of pioneering concept that Fogarty Innovation fosters.”

“Raydiant has assembled a team that is uniquely qualified to develop LUMERAH and provide obstetricians with accurate, quantifiable data for making critical labor and delivery decisions. When this device shows to improve the health of mothers and newborns, we are hopeful it will become the standard in hospitals worldwide,” said Linda Greub, Managing Partner of Avestria Ventures.

Raydiant Oximetry plans to use the proceeds of the Series A2 financing to complete a clinical study at the University of Texas Medical Branch (UTMB) in Galveston, Texas. UTMB is one of 12 clinical research centers established by the NIH Maternal-Fetal-Medicine Network to promote clinical studies during pregnancy. The principal investigator for the study is Dr. George Saade, the Chief of Maternal Fetal Medicine at UTMB.

“We are very pleased that LUMERAH continues to resonate with our audiences, including clinicians and investors,” said Dr. Neil P. Ray. “We will continue to create shareholder value by demonstrating the clinical utility of LUMERAH and look forward to the transformative impact this technology will have on the field, physicians and their patients.”

 

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”