Flexuspine, Inc.
Country not established
- Devices
- 1
What Flexuspine, Inc. makes
Flexuspine, Inc. manufactures the EXPANSE Vertebral Body Replacement Device, a spinal implant designed for vertebral body replacement procedures.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Expanse Vertebral Body Replacement Device Ref K050997
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flexuspine, Inc. have in the registry?
The registry currently lists 1 device for Flexuspine, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flexuspine, Inc.'s devices?
Among its 1 most recently registered device, Flexuspine, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Flexuspine, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Flexuspine, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flexuspine, Inc. in the registry?
The most recently registered devices listed for Flexuspine, Inc. include EXPANSE VERTEBRAL BODY REPLACEMENT DEVICE.