Kgt, Inc.
Country not established
- Devices
- 1
What Kgt, Inc. makes
Kgt, Inc. manufactures the BF-NAVI, a medical imaging device designed for intraoperative navigation and guidance, likely used in surgical procedures to enhance precision and reduce complications.
The BF-NAVI falls under FDA Class II regulation and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Bf-Navi Ref K093810
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kgt, Inc. have in the registry?
The registry currently lists 1 device for Kgt, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kgt, Inc.'s devices?
Among its 1 most recently registered device, Kgt, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kgt, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kgt, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kgt, Inc. in the registry?
The most recently registered devices listed for Kgt, Inc. include BF-NAVI.