Neurolumen LLC
Country not established FDA establishment FEI 3010144038
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Neurolumen Pn-1000 Ref K142025
510(k) 510(k)Neutrolumenpn System, Model 1000 Ref K082223
510(k) 510(k)
Company details
- FDA FEI number
- 3010144038
- Address
- 9636 N May Ave Ste 230, Oklahoma City, OK, 73120
Frequently asked questions
How many devices does NEUROLUMEN LLC have in the registry?
The registry currently lists 2 devices for NEUROLUMEN LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEUROLUMEN LLC's devices?
Among its 2 most recently registered devices, NEUROLUMEN LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do NEUROLUMEN LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for NEUROLUMEN LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NEUROLUMEN LLC in the registry?
The most recently registered devices listed for NEUROLUMEN LLC include NEUROLUMEN PN-1000 and NEUTROLUMENPN SYSTEM, MODEL 1000.