H2, Inc.
Country not established
- Devices
- 1
What H2, Inc. makes
H2, Inc. develops a mobile application and companion smart cable designed for remote patient monitoring and data transmission, enabling real-time health metrics tracking.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The products are listed in the FDA’s 510(k) database and are based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does H2, Inc. have in the registry?
The registry currently lists 1 device for H2, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list H2, Inc.'s devices?
Among its 1 most recently registered device, H2, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do H2, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for H2, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from H2, Inc. in the registry?
The most recently registered devices listed for H2, Inc. include HEALTH2SYNC MOBILE APPLICATION, HEALTH2SYNC SMART CABLE.