Navifus Corporation
TaiwanFDA applicant, unverified
- Devices
- 1
What Navifus Corporation makes
Navifus Corporation manufactures the NAVIRFA Scope, a device designed for intraoperative imaging and navigation in surgical procedures, aiding in precise anatomical visualization and guidance.
The NAVIRFA Scope is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
NAVIRFA Scope Ref K211529
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Navifus Corporation have in the registry?
The registry currently lists 1 device for Navifus Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Navifus Corporation's devices?
Among its 1 most recently registered device, Navifus Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Navifus Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Navifus Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Navifus Corporation in the registry?
The most recently registered devices listed for Navifus Corporation include NAVIRFA Scope.