Visijet, Inc.
Country not established
- Devices
- 1
What Visijet, Inc. makes
Visijet, Inc. manufactures the VISIJET HYDROKERATOME, Model 50, a device used for cutting corneal tissue in ophthalmic procedures.
The device is classified as Class I under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Visijet Hydrokeratome, Model 50 Ref K991124
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visijet, Inc. have in the registry?
The registry currently lists 1 device for Visijet, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visijet, Inc.'s devices?
Among its 1 most recently registered device, Visijet, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Visijet, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Visijet, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Visijet, Inc. in the registry?
The most recently registered devices listed for Visijet, Inc. include VISIJET HYDROKERATOME, MODEL 50.