Ultrasound AI
Country not established
- Devices
- 1
What Ultrasound AI makes
Ultrasound AI develops an AI-powered software tool called Delivery Date AI, designed to assist in predicting gestational age and estimated delivery dates using ultrasound imaging.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The products are based in the United States.
Catalogue
Delivery Date AI Ref DEN250007
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Ultrasound AI have in the registry?
The registry currently lists 1 device for Ultrasound AI. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultrasound AI's devices?
Among its 1 most recently registered device, Ultrasound AI has devices listed in FDA 510(k) (1 device).
What risk classes do Ultrasound AI's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultrasound AI's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultrasound AI in the registry?
The most recently registered devices listed for Ultrasound AI include Delivery Date AI.