Neurolign USA, LLC
Country not established
- Devices
- 1
What Neurolign USA, LLC makes
Neurolign USA, LLC makes neuro-otologic test centers, video nystagmography systems, and portable assessment systems for nystagmography, including the I-Portal Neuro Otologic Test Center, I-Portal Video Nystagmography System, and I-Portal Portable Assessment System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurolign USA, LLC have in the registry?
The registry currently lists 1 device for Neurolign USA, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurolign USA, LLC's devices?
Among its 1 most recently registered device, Neurolign USA, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Neurolign USA, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurolign USA, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurolign USA, LLC in the registry?
The most recently registered devices listed for Neurolign USA, LLC include I-Portal Neuro Otologic Test Center, I-Portal Video Nystagmography System, I-Portal Portable Assessment System - Nysragmograph.