Endobionics, Inc.
Country not established
- Devices
- 1
What Endobionics, Inc. makes
Endobionics, Inc. manufactures the Endobionics Microsyringe Infusion Catheter, a device designed for precise drug delivery via infusion.
The company’s portfolio is regulated under FDA Class II and includes devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endobionics, Inc. have in the registry?
The registry currently lists 1 device for Endobionics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endobionics, Inc.'s devices?
Among its 1 most recently registered device, Endobionics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Endobionics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endobionics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endobionics, Inc. in the registry?
The most recently registered devices listed for Endobionics, Inc. include ENDOBIONICS MICROSYRINGE (USYRINGE) INFUSION CATHETER.