Jintronix, Inc.
Country not established FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Jintronix, Inc. makes
Jintronix, Inc. manufactures the Jintronix Rehabilitation System (JRS), a device designed for rehabilitation purposes, likely incorporating technologies to support physical therapy or motor function recovery.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. Jintronix is based in the United States.
Catalogue
Jintronix Rehabilitation System (Jrs) Ref K130847
Regimes: 510(k) Registry: 510(k)Jintronix Ref K143034
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Jintronix Inc. Montreal Quebec · CA FEI 3011197286
Frequently asked questions
How many devices does Jintronix, Inc. have in the registry?
The registry currently lists 2 devices for Jintronix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jintronix, Inc.'s devices?
Among its 2 most recently registered devices, Jintronix, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Jintronix, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Jintronix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jintronix, Inc. in the registry?
The most recently registered devices listed for Jintronix, Inc. include JINTRONIX REHABILITATION SYSTEM (JRS) and Jintronix.
Which FDA establishments are linked to Jintronix, Inc.?
1 FDA establishment is linked to Jintronix, Inc. in the registry; they are listed on the company page.