Neuroregen, LLC
Country not established
- Devices
- 1
What Neuroregen, LLC makes
Neuroregen, LLC manufactures the NEUROTUBE, a medical device designed for neural regeneration or nerve repair applications.
The NEUROTUBE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Neurotube Ref K983007
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuroregen, LLC have in the registry?
The registry currently lists 1 device for Neuroregen, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuroregen, LLC's devices?
Among its 1 most recently registered device, Neuroregen, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Neuroregen, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuroregen, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuroregen, LLC in the registry?
The most recently registered devices listed for Neuroregen, LLC include NEUROTUBE.