Reneau, Inc.
Country not established
- Devices
- 1
What Reneau, Inc. makes
Reneau, Inc. manufactures the Reneau Unit, a medical device designed for [specific application not detailed in provided data].
The company’s portfolio is regulated under Class II devices in the U.S. and includes products listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Reneau Unit Ref K840841
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Reneau, Inc. have in the registry?
The registry currently lists 1 device for Reneau, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reneau, Inc.'s devices?
Among its 1 most recently registered device, Reneau, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Reneau, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Reneau, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reneau, Inc. in the registry?
The most recently registered devices listed for Reneau, Inc. include RENEAU UNIT.