Method Mobility
Country not established
- Devices
- 4
What Method Mobility makes
Method Mobility manufactures ambulatory patient monitoring systems, including the AMP and AMP Plus devices. These products are designed for continuous, wireless monitoring of vital signs such as heart rate, blood pressure, and oxygen saturation, supporting remote patient observation and mobility during recovery or treatment.
The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Method Mobility have in the registry?
The registry currently lists 4 devices for Method Mobility. Devices recorded under merged duplicate company entries are counted once.
Which registries list Method Mobility's devices?
Among its 4 most recently registered devices, Method Mobility has devices listed in FDA 510(k) (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Method Mobility's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Method Mobility's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Method Mobility in the registry?
The most recently registered devices listed for Method Mobility include AMP plus, AMP, AMP js and AMP by Method Mobility, AMP Plus (or +) by Method Mobility.