Kw Ear Lab, Inc.
Country not established
- Devices
- 1
What Kw Ear Lab, Inc. makes
Kw Ear Lab, Inc. manufactures the REVE134, a medical device designed for ear-related applications, though specific use cases are not detailed in the provided data.
The REVE134 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
REVE134 Ref K151719
510(k) 510(k)
Frequently asked questions
How many devices does Kw Ear Lab, Inc. have in the registry?
The registry currently lists 1 device for Kw Ear Lab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kw Ear Lab, Inc.'s devices?
Among its 1 most recently registered device, Kw Ear Lab, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kw Ear Lab, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kw Ear Lab, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kw Ear Lab, Inc. in the registry?
The most recently registered devices listed for Kw Ear Lab, Inc. include REVE134.