Evit Labs, Inc.
Country not established
- Devices
- 1
What Evit Labs, Inc. makes
Evit Labs, Inc. manufactures the SONIK LDI 20 AIR device, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Sonik Ldi 20 Air Ref K030374
510(k) 510(k)
Frequently asked questions
How many devices does Evit Labs, Inc. have in the registry?
The registry currently lists 1 device for Evit Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Evit Labs, Inc.'s devices?
Among its 1 most recently registered device, Evit Labs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Evit Labs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Evit Labs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Evit Labs, Inc. in the registry?
The most recently registered devices listed for Evit Labs, Inc. include SONIK LDI 20 AIR.