Mediott, Inc.
JapanFDA applicant, unverified
- Devices
- 2
What Mediott, Inc. makes
Mediott, Inc. manufactures the RW-1, a reusable medical device designed for wound irrigation and debridement in clinical settings.
The RW-1 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Frequently asked questions
How many devices does Mediott, Inc. have in the registry?
The registry currently lists 2 devices for Mediott, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediott, Inc.'s devices?
Among its 2 most recently registered devices, Mediott, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mediott, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mediott, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediott, Inc. in the registry?
The most recently registered devices listed for Mediott, Inc. include RW-1.