Inrange Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Inrange Systems, Inc. makes
Inrange Systems, Inc. manufactures the Inrange Remote Medication Management System, a device designed for monitoring and managing medication adherence remotely, and EMMA, a system for electronic medication management and monitoring.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Inrange Remote Medication Management System Ref DEN060002
Regimes: De Novo Registry: De NovoEmma Ref K150174
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inrange Systems, Inc. have in the registry?
The registry currently lists 2 devices for Inrange Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inrange Systems, Inc.'s devices?
Among its 2 most recently registered devices, Inrange Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Inrange Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Inrange Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inrange Systems, Inc. in the registry?
The most recently registered devices listed for Inrange Systems, Inc. include INRANGE REMOTE MEDICATION MANAGEMENT SYSTEM and EMMA.