Tko, Inc.
Country not established
- Devices
- 1
What Tko, Inc. makes
Tko, Inc. makes medical devices such as the PRO-CHILL STIMPACK.
The company's portfolio, which includes Class II devices, is listed in the FDA 510(k) registry and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Pro-Chill Stimpack Ref K912210
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tko, Inc. have in the registry?
The registry currently lists 1 device for Tko, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tko, Inc.'s devices?
Among its 1 most recently registered device, Tko, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tko, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tko, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tko, Inc. in the registry?
The most recently registered devices listed for Tko, Inc. include PRO-CHILL STIMPACK.