Self Driving Ultrasound

TECHNOLOGY

Autonomous, hands-free ultrasound

Bloom Standard’s RAPIDscan Ultrasound System has received FDA Breakthrough Device Designation. The Device is pending FDA approval and has not been authorized or cleared by the FDA. Investigational Device, Limited by Federal Law to Investigational Use.

01 / PROBLEM

90% of children lack access to ultrasound imaging in their local medical settings

Delayed detection of respiratory + cardiac conditions are among the most common killers of babies + children, responsible for nearly 1/3 of under-5 deaths globally.

Between 60-75% of these deaths could be prevented through earlier detection and rapid assessment of their condition.

Most existing newborn, pediatric and maternal ultrasound solutions are expensive, immobile and can only be used in high-level medical setting by highly skilled health staff

02 / SOLUTION

Autonomous, hands-free ultrasound scans - any user, anywhere

Simple hands free RAPID scan, to earlier detect heart or lung abnormalities in maternity, primary care, underserved, under-resourced, humanitarian and front line health settings

AI-driven onboard image interpretation = real time decision support, timely referrals, lifesaving interventions + conservation of essential health resources

03 / IMPACT

Reduce mortality and poor outcomes tied to delayed detection of lung + cardiac conditions

Bolsters health access + equity for medically fragile children

Integrates with existing health systems + public health initiatives

Ends excessive use of potentially-harmful x-ray imaging in children

10X cost savings over traditional ultrasound solutions

Product

ABOUT BLOOM

OUR STORY

Developed by parents of a child with CHD (Congenital Heart Defect), Bloom Standard is more than just another device, it's a passion that has followed our team around the world.