Tridak
Country not established
- Devices
- 1
What Tridak makes
Tridak manufactures the STEPPER, which is a device used for fluid dispensing applications.
The company is based in the US, and its portfolio includes Class I devices that are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Stepper Ref K771539
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tridak have in the registry?
The registry currently lists 1 device for Tridak. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tridak's devices?
Among its 1 most recently registered device, Tridak has devices listed in FDA 510(k) (1 device).
What risk classes do Tridak's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tridak's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tridak in the registry?
The most recently registered devices listed for Tridak include STEPPER.