Ultramind International, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Ultramind International, Ltd. makes
Ultramind International, Ltd. manufactures biofeedback systems designed to promote relaxation, including the RELAXPLUS device and the ULTRAMIND BIOFEEDBACK SYSTEM with DE-STRESS software. These products use physiological monitoring to provide real-time feedback for stress reduction and relaxation training.
The company’s portfolio is classified under FDA Class II devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Relaxplus Ref K951213
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultramind International, Ltd. have in the registry?
The registry currently lists 2 devices for Ultramind International, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultramind International, Ltd.'s devices?
Among its 2 most recently registered devices, Ultramind International, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ultramind International, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ultramind International, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultramind International, Ltd. in the registry?
The most recently registered devices listed for Ultramind International, Ltd. include RELAXPLUS and ULTRAMIND BIOFEEDBACK SYSTEM WITH DE-STRESS SOFTWARE.