Avidhrt, Inc.
Country not established
- Devices
- 1
What Avidhrt, Inc. makes
Avidhrt, Inc. manufactures the Avidhrt Sense SpO2, a pulse oximetry device designed to measure oxygen saturation in blood (SpO2) non-invasively.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Avidhrt Sense SpO2 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
Avidhrt Sense SpO2 Ref K241086
510(k) 510(k)
Frequently asked questions
How many devices does Avidhrt, Inc. have in the registry?
The registry currently lists 1 device for Avidhrt, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avidhrt, Inc.'s devices?
Among its 1 most recently registered device, Avidhrt, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Avidhrt, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Avidhrt, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avidhrt, Inc. in the registry?
The most recently registered devices listed for Avidhrt, Inc. include Avidhrt Sense SpO2.