Cbyon, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cbyon, Inc. makes
Cbyon, Inc. makes the CBYON Surgical Operating System (SOS) and the CBYON System with Image Enhanced Fluoroscopy Module.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Cbyon Surgical Operating System (Sos) Ref K000171
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cbyon, Inc. have in the registry?
The registry currently lists 2 devices for Cbyon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cbyon, Inc.'s devices?
Among its 2 most recently registered devices, Cbyon, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cbyon, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cbyon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cbyon, Inc. in the registry?
The most recently registered devices listed for Cbyon, Inc. include CBYON SURGICAL OPERATING SYSTEM (SOS) and CBYON SYSTEM WITH IMAGE ENHANCED FLUOROSCOPY MODULE.