Jfi Endineering, Inc.
Country not established
- Devices
- 1
What Jfi Endineering, Inc. makes
Jfi Engineering, Inc. manufactures the Jennings Javelin, a medical device designed for surgical or procedural applications, likely within orthopedic or trauma surgery given the naming convention.
The Jennings Javelin is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Jennings Javelin Ref K942548
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jfi Endineering, Inc. have in the registry?
The registry currently lists 1 device for Jfi Endineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jfi Endineering, Inc.'s devices?
Among its 1 most recently registered device, Jfi Endineering, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jfi Endineering, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jfi Endineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jfi Endineering, Inc. in the registry?
The most recently registered devices listed for Jfi Endineering, Inc. include JENNINGS JAVELIN.