Medo U.S.A., Inc.
Country not established
- Devices
- 2
What Medo U.S.A., Inc. makes
Medo U.S.A., Inc. manufactures bubble bath systems, specifically the MA-80, 400, 600, and 700 models, as well as the Medomer MBF-100 II device.
These products are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Medo Bubble Bath Ma-80, 400, 600 & 700 Ref K844064
Regimes: 510(k) Registry: 510(k)Medo Medomer Mbf-100 Ii Ref K841235
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medo U.S.A., Inc. have in the registry?
The registry currently lists 2 devices for Medo U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medo U.S.A., Inc.'s devices?
Among its 2 most recently registered devices, Medo U.S.A., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medo U.S.A., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medo U.S.A., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medo U.S.A., Inc. in the registry?
The most recently registered devices listed for Medo U.S.A., Inc. include MEDO BUBBLE BATH MA-80, 400, 600 & 700 and MEDO MEDOMER MBF-100 II.