Kneevoice, Inc.
Country not established
- Devices
- 1
What Kneevoice, Inc. makes
Kneevoice, Inc. manufactures the Kneevoice Cartilage Evaluation System, a diagnostic device designed for assessing cartilage integrity in knee joints. The system likely integrates imaging or sensor technology to provide objective evaluations of cartilage condition, aiding in clinical decision-making for joint health assessments.
The Kneevoice Cartilage Evaluation System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kneevoice, Inc. have in the registry?
The registry currently lists 1 device for Kneevoice, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kneevoice, Inc.'s devices?
Among its 1 most recently registered device, Kneevoice, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kneevoice, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kneevoice, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kneevoice, Inc. in the registry?
The most recently registered devices listed for Kneevoice, Inc. include Kneevoice Cartilage Evaluation System (750-3600-001).