Mikado Ca.
Country not established
- Devices
- 1
What Mikado Ca. makes
Mikado Ca. makes spectacle frames, which are a type of medical device.
The company's portfolio, including its spectacle frames, is regulated as a Class I device and is listed in the FDA 510k registry, with the company based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Spectacle Frames Ref K914413
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mikado Ca. have in the registry?
The registry currently lists 1 device for Mikado Ca.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mikado Ca.'s devices?
Among its 1 most recently registered device, Mikado Ca. has devices listed in FDA 510(k) (1 device).
What risk classes do Mikado Ca.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mikado Ca.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mikado Ca. in the registry?
The most recently registered devices listed for Mikado Ca. include SPECTACLE FRAMES.