Bright Spine
Country not established
- Devices
- 3
What Bright Spine makes
Bright Spine manufactures the Galileo Vertebral Body Replacement Device, a spinal implant designed for vertebral body replacement in surgical procedures.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The devices are listed in the FDA’s 510(k) registry. Bright Spine is based in the United States.
Catalogue
Bright Spine Galileo Spinal Spacer System Ref K102449
510(k) 510(k)Galileo Vertebral Body Replacement Device Ref K221542
510(k) 510(k)Galileo Vertebral Body Replacement Device Ref K192145
510(k) 510(k)
Frequently asked questions
How many devices does Bright Spine have in the registry?
The registry currently lists 3 devices for Bright Spine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bright Spine's devices?
Among its 3 most recently registered devices, Bright Spine has devices listed in FDA 510(k) (3 devices).
What risk classes do Bright Spine's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bright Spine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bright Spine in the registry?
The most recently registered devices listed for Bright Spine include BRIGHT SPINE GALILEO SPINAL SPACER SYSTEM and Galileo Vertebral Body Replacement Device.