Orbital Research, Inc.
Country not established
- Devices
- 1
What Orbital Research, Inc. makes
Orbital Research, Inc. manufactures the ORI F6T dry ECG monitoring electrode, a reusable adhesive-free electrode designed for continuous cardiac monitoring without gel or skin preparation.
The company’s product portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance in the United States. The company is based in the US.
Catalogue
Ori F6T Dry Ecg Monitoring Electrode Ref K062760
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orbital Research, Inc. have in the registry?
The registry currently lists 1 device for Orbital Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orbital Research, Inc.'s devices?
Among its 1 most recently registered device, Orbital Research, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orbital Research, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orbital Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orbital Research, Inc. in the registry?
The most recently registered devices listed for Orbital Research, Inc. include ORI F6T DRY ECG MONITORING ELECTRODE.