Imexco General, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Imexco General, Ltd. makes
Imexco General, Ltd. manufactures the NEURITOR 2001, a device designed for neurostimulation or neuromodulation applications, likely targeting specific neurological or pain management conditions.
The NEURITOR 2001 is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Neuritor 2001 Ref K902752
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Imexco General, Ltd. have in the registry?
The registry currently lists 1 device for Imexco General, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imexco General, Ltd.'s devices?
Among its 1 most recently registered device, Imexco General, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Imexco General, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Imexco General, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imexco General, Ltd. in the registry?
The most recently registered devices listed for Imexco General, Ltd. include NEURITOR 2001.