In-X Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What In-X Corp. makes
In-X Corp. manufactures the Home-Away System, a portable patient monitoring device designed for use in home healthcare settings, and the Minolta Pulsox-3 and Pulsox-3I, pulse oximeters for measuring oxygen saturation and pulse rate. These devices are intended for non-invasive monitoring of vital signs in clinical and ambulatory environments.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Home-Away System, Model 1041 Ref K042944
Regimes: 510(k) Registry: 510(k)Home-Away System Ref K004047
Regimes: 510(k) Registry: 510(k)Minolta Pulsox-3/Minolta Pulsox-3I Ref K984570
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does In-X Corp. have in the registry?
The registry currently lists 3 devices for In-X Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list In-X Corp.'s devices?
Among its 3 most recently registered devices, In-X Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do In-X Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for In-X Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from In-X Corp. in the registry?
The most recently registered devices listed for In-X Corp. include HOME-AWAY SYSTEM, MODEL 1041, HOME-AWAY SYSTEM and MINOLTA PULSOX-3/MINOLTA PULSOX-3I.