Omnllife Science, Inc.
Country not established
- Devices
- 1
What Omnllife Science, Inc. makes
Omnllife Science, Inc. manufactures the OMNIBotics Knee System, a device designed for knee replacement or joint reconstruction procedures.
The OMNIBotics Knee System 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
OMNIBotics Knee System Ref K163338
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omnllife Science, Inc. have in the registry?
The registry currently lists 1 device for Omnllife Science, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omnllife Science, Inc.'s devices?
Among its 1 most recently registered device, Omnllife Science, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Omnllife Science, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omnllife Science, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omnllife Science, Inc. in the registry?
The most recently registered devices listed for Omnllife Science, Inc. include OMNIBotics Knee System.