Isag Rx, Inc.
Country not established
- Devices
- 1
What Isag Rx, Inc. makes
Isag Rx, Inc. manufactures the iSage Rx system, a digital tool designed for basal insulin titration in diabetes management. The device assists users in adjusting insulin doses based on automated recommendations and glucose monitoring data, aiming to improve glycemic control through personalized algorithms.
The iSage Rx system is classified as a Class II medical device in the U.S. and is authorised through the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
iSage Rx (iSage Rx Basal Insulin Titration) Ref K161865
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Isag Rx, Inc. have in the registry?
The registry currently lists 1 device for Isag Rx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Isag Rx, Inc.'s devices?
Among its 1 most recently registered device, Isag Rx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Isag Rx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Isag Rx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Isag Rx, Inc. in the registry?
The most recently registered devices listed for Isag Rx, Inc. include iSage Rx (iSage Rx Basal Insulin Titration).