Wolfline Corp.
Country not established
- Devices
- 1
What Wolfline Corp. makes
Wolfline Corp. manufactures the WAVE GATE, which is a medical device.
The company is based in the US, and its product is regulated as a Class II device listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Wave Gate Ref K853412
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wolfline Corp. have in the registry?
The registry currently lists 1 device for Wolfline Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wolfline Corp.'s devices?
Among its 1 most recently registered device, Wolfline Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Wolfline Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wolfline Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wolfline Corp. in the registry?
The most recently registered devices listed for Wolfline Corp. include WAVE GATE.