Rowenta, Inc.
Country not established
- Devices
- 1
What Rowenta, Inc. makes
Rowenta, Inc. manufactures the Rowenta Inc. Bodypartner Vision (Model BM 210), a device designed for vision correction or eye health monitoring, likely targeting non-invasive or low-risk optical or diagnostic applications.
The device falls under FDA Class II regulation and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rowenta, Inc. have in the registry?
The registry currently lists 1 device for Rowenta, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rowenta, Inc.'s devices?
Among its 1 most recently registered device, Rowenta, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rowenta, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rowenta, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rowenta, Inc. in the registry?
The most recently registered devices listed for Rowenta, Inc. include ROWENTA INC. BODYPARTNER VISION, MODEL BM 210 (2079565620).