Product DevelopmentDaxor is developing a next-generation BVA that is more than three times faster and capable of providing full results at the bedside, with FDA approval expected in 2025.
Regulatory StrategyThe decision to pivot to a single 510(k) submission, rather than a dual CLIA waiver approach, is a prudent regulatory strategy that reduces data burden and accelerates the approval timeline.
Revenue GrowthThe company reported strong revenue growth of +117% in its blood volume business across leading medical centers in the U.S.