Cleanblade, Inc.
Country not established
- Devices
- 1
What Cleanblade, Inc. makes
Cleanblade, Inc. manufactures the CLEANBLADE, a surgical device designed for precise tissue cutting and sealing in minimally invasive procedures.
The CLEANBLADE is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cleanblade Ref K931480
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cleanblade, Inc. have in the registry?
The registry currently lists 1 device for Cleanblade, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cleanblade, Inc.'s devices?
Among its 1 most recently registered device, Cleanblade, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cleanblade, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cleanblade, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cleanblade, Inc. in the registry?
The most recently registered devices listed for Cleanblade, Inc. include CLEANBLADE.