Orthohub, Inc.
Country not established
- Devices
- 1
What Orthohub, Inc. makes
Orthohub, Inc. develops software designed for external fixation systems, supporting surgical planning and intraoperative guidance in orthopedic procedures.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. Orthohub, Inc. is based in the United States.
Catalogue
Orthohub External Fixator Software Ref K140550
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthohub, Inc. have in the registry?
The registry currently lists 1 device for Orthohub, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthohub, Inc.'s devices?
Among its 1 most recently registered device, Orthohub, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthohub, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthohub, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthohub, Inc. in the registry?
The most recently registered devices listed for Orthohub, Inc. include ORTHOHUB EXTERNAL FIXATOR SOFTWARE.