Voxel Ray Solutions, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3036107971
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Voxel Ray Solutions, LLC makes
VOXEL Ray Solutions, LLC manufactures the GentleBeam (GB1000), a medical device designed for precise radiation therapy applications, likely targeting superficial tumors or skin lesions with controlled dose delivery.
The GentleBeam (GB1000) is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
GentleBeam (GB1000) Ref K250692
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3036107971
- Address
- 200 S Frontage Rd Ste 200, Burr Ridge, IL, 60527
Frequently asked questions
How many devices does VOXEL RAY SOLUTIONS, LLC have in the registry?
The registry currently lists 1 device for VOXEL RAY SOLUTIONS, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list VOXEL RAY SOLUTIONS, LLC's devices?
Among its 1 most recently registered device, VOXEL RAY SOLUTIONS, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do VOXEL RAY SOLUTIONS, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for VOXEL RAY SOLUTIONS, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VOXEL RAY SOLUTIONS, LLC in the registry?
The most recently registered devices listed for VOXEL RAY SOLUTIONS, LLC include GentleBeam (GB1000).