Empnia, Inc.
Country not established
- Devices
- 40
What Empnia, Inc. makes
Empnia, Inc. manufactures the eMotus Respiratory Motion Management System, a device designed to monitor and manage respiratory motion for precise imaging and diagnostic procedures.
The company’s portfolio is regulated under FDA Class II devices, with the eMotus system authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Search and filter all 40 devicesCompany details
- DUNS number
- 119402293
Frequently asked questions
How many devices does Empnia, Inc. have in the registry?
The registry currently lists 40 devices for Empnia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Empnia, Inc.'s devices?
Among its 40 most recently registered devices, Empnia, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (39 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Empnia, Inc.'s devices fall under?
Among its 40 most recently registered devices, the classes recorded for Empnia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Empnia, Inc. in the registry?
The most recently registered devices listed for Empnia, Inc. include eMotus EMP001, eMotus EMP002, eMotus EMP101 and eMotus EMP103.