Timocco USA, Inc.
Country not established
- Devices
- 1
What Timocco USA, Inc. makes
Timocco USA, Inc. develops virtual-display software designed for routine exercise therapy, including digital platforms that guide users through structured rehabilitation or skill-building routines. Their products focus on delivering interactive, screen-based exercises to support physical or cognitive recovery.
The company’s portfolio is classified under FDA’s Class II medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. Timocco USA, Inc. is based in the United States.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 090141480
Frequently asked questions
How many devices does TIMOCCO USA, INC. have in the registry?
The registry currently lists 1 device for TIMOCCO USA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TIMOCCO USA, INC.'s devices?
Among its 1 most recently registered device, TIMOCCO USA, INC. has devices listed in FDA GUDID (1 device).
What risk classes do TIMOCCO USA, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for TIMOCCO USA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TIMOCCO USA, INC. in the registry?
The most recently registered devices listed for TIMOCCO USA, INC. include Restore Skills Therapy 1.