T.F. Herceg, Inc.
Country not established
- Devices
- 1
What T.F. Herceg, Inc. makes
T.F. Herceg, Inc. manufactures the HANDI-MOVE, a device designed for mobility assistance, likely intended for patients requiring aid in movement or positioning.
The company’s portfolio is regulated under FDA Class II devices, with the HANDI-MOVE authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Handi-Move Ref K854461
510(k) 510(k)
Frequently asked questions
How many devices does T.F. Herceg, Inc. have in the registry?
The registry currently lists 1 device for T.F. Herceg, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list T.F. Herceg, Inc.'s devices?
Among its 1 most recently registered device, T.F. Herceg, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do T.F. Herceg, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for T.F. Herceg, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from T.F. Herceg, Inc. in the registry?
The most recently registered devices listed for T.F. Herceg, Inc. include HANDI-MOVE.