Nelis
Country not established
- Devices
- 2
What Nelis makes
Nelis manufactures medical devices including the Endo Keeper and GLOVE PORT, which are Class II devices.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Endo Keeper Ref K152598
Regimes: 510(k) Registry: 510(k)Glove Port Ref K141715
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nelis have in the registry?
The registry currently lists 2 devices for Nelis. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nelis's devices?
Among its 2 most recently registered devices, Nelis has devices listed in FDA 510(k) (2 devices).
What risk classes do Nelis's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nelis's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nelis in the registry?
The most recently registered devices listed for Nelis include Endo Keeper and GLOVE PORT.