Mosie Baby
Country not established
- Devices
- 1
What Mosie Baby makes
Mosie Baby produces a wearable baby monitoring kit designed for real-time tracking of infant movement and sleep patterns, intended for use in home environments.
The company’s product is classified as Class II under FDA regulations and is listed via a 510(k) clearance. Mosie Baby is based in the United States.
Catalogue
Mosie Baby Kit Ref K231203
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mosie Baby have in the registry?
The registry currently lists 1 device for Mosie Baby. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mosie Baby's devices?
Among its 1 most recently registered device, Mosie Baby has devices listed in FDA 510(k) (1 device).
What risk classes do Mosie Baby's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mosie Baby's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mosie Baby in the registry?
The most recently registered devices listed for Mosie Baby include Mosie Baby Kit.