Gensia, Inc.
Country not established
- Devices
- 1
What Gensia, Inc. makes
Gensia, Inc. manufactures the GENESA System, a medical device designed for use in specific surgical procedures requiring precise imaging and guidance.
The company’s portfolio is regulated under Class III designation in the US, with the GENESA System listed under a Premarket Approval (PMA) application with the FDA. The company is based in the United States.
Catalogue
Genesa(R) System Ref P940001
Regimes: PMA, withdrawn Registry: PMA
Frequently asked questions
How many devices does Gensia, Inc. have in the registry?
The registry currently lists 1 device for Gensia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gensia, Inc.'s devices?
Among its 1 most recently registered device, Gensia, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Gensia, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gensia, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Gensia, Inc. in the registry?
The most recently registered devices listed for Gensia, Inc. include GENESA(R) SYSTEM.