Bioanalogics, Inc.
Country not established
- Devices
- 1
What Bioanalogics, Inc. makes
Bioanalogics, Inc. manufactures the Edema System, a medical device designed for the management and monitoring of edema, likely targeting conditions such as lymphedema or post-surgical fluid retention.
The Edema System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is headquartered in the United States.
Catalogue
Edema System Ref K962783
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioanalogics, Inc. have in the registry?
The registry currently lists 1 device for Bioanalogics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioanalogics, Inc.'s devices?
Among its 1 most recently registered device, Bioanalogics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bioanalogics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bioanalogics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioanalogics, Inc. in the registry?
The most recently registered devices listed for Bioanalogics, Inc. include EDEMA SYSTEM.