Oreon Technologies, Inc.
Country not established
- Devices
- 2
What Oreon Technologies, Inc. makes
Oreon Technologies, Inc. manufactures the Enovare Ultrasound System, a medical imaging device designed for diagnostic ultrasound procedures. This system is intended for visualizing internal body structures, aiding in the assessment of organs, tissues, and potential abnormalities.
The Enovare Ultrasound System is classified as a Class II device under FDA regulations and has undergone the 510(k) clearance process. The company is based in the United States.
Catalogue
- Registry: GUDID
Enovare Ultrasound System Ref K153620
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 054353531
- [email protected]
- Phone
- 19144130087
Frequently asked questions
How many devices does Oreon Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Oreon Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oreon Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Oreon Technologies, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Oreon Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oreon Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oreon Technologies, Inc. in the registry?
The most recently registered devices listed for Oreon Technologies, Inc. include Enovare 4001001 and Enovare Ultrasound System.