Gi Bionics, LLC
Country not established
- Devices
- 1
What Gi Bionics, LLC makes
Gi Bionics, LLC manufactures the Fecobionics Anorectal System, a medical device designed for anorectal function assessment and treatment.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Fecobionics Anorectal System Ref K242666
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gi Bionics, LLC have in the registry?
The registry currently lists 1 device for Gi Bionics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gi Bionics, LLC's devices?
Among its 1 most recently registered device, Gi Bionics, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Gi Bionics, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gi Bionics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gi Bionics, LLC in the registry?
The most recently registered devices listed for Gi Bionics, LLC include Fecobionics Anorectal System.