Sanofi, Inc.
Country not established
- Devices
- 1
What Sanofi, Inc. makes
Sanofi, Inc. manufactures My Dose Coach, a digital tool designed to support medication adherence by providing reminders and tracking for patients.
The device falls under FDA Class II regulation and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
My Dose Coach Ref K163099
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanofi, Inc. have in the registry?
The registry currently lists 1 device for Sanofi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanofi, Inc.'s devices?
Among its 1 most recently registered device, Sanofi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sanofi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sanofi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanofi, Inc. in the registry?
The most recently registered devices listed for Sanofi, Inc. include My Dose Coach.