Neuralytix, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Neuralytix, LLC makes
Neuralytix, LLC manufactures the Neuralytix iD3 System (NTX-9001), a device designed for intraoperative neurophysiological monitoring to assess neural function during surgical procedures.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
iD3 Nav Decompression Probe (NTX-9005) Ref K260992
Regimes: 510(k) Registry: 510(k)Neuralytix iD3 System (NTX-9001) Ref K243636
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuralytix, LLC have in the registry?
The registry currently lists 2 devices for Neuralytix, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuralytix, LLC's devices?
Among its 2 most recently registered devices, Neuralytix, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Neuralytix, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neuralytix, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuralytix, LLC in the registry?
The most recently registered devices listed for Neuralytix, LLC include iD3 Nav Decompression Probe (NTX-9005) and Neuralytix iD3 System (NTX-9001).