Retec USA, Inc.
Country not established
- Devices
- 1
What Retec USA, Inc. makes
Retec USA, Inc. manufactures the HI-RIDER wheelchair, a mobility device designed for users requiring manual or assisted propulsion.
The company’s products are regulated as Class II medical devices in the US and are listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Hi-Rider Wheelchair Ref K890695
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retec USA, Inc. have in the registry?
The registry currently lists 1 device for Retec USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retec USA, Inc.'s devices?
Among its 1 most recently registered device, Retec USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Retec USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Retec USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retec USA, Inc. in the registry?
The most recently registered devices listed for Retec USA, Inc. include HI-RIDER WHEELCHAIR.