Ikeeps, Inc.
Country not established
- Devices
- 1
What Ikeeps, Inc. makes
Ikeeps, Inc. manufactures the ICASE, a medical device designed for continuous glucose monitoring and insulin delivery integration, supporting automated insulin dosing for diabetic patients.
The ICASE is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Icase Ref K021248
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ikeeps, Inc. have in the registry?
The registry currently lists 1 device for Ikeeps, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ikeeps, Inc.'s devices?
Among its 1 most recently registered device, Ikeeps, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ikeeps, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ikeeps, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ikeeps, Inc. in the registry?
The most recently registered devices listed for Ikeeps, Inc. include ICASE.