Beamline Corporation
Country not established
- Devices
- 1
What Beamline Corporation makes
Beamline Corporation manufactures the BEAMER PAINLOW Infrared Light Treatment System, a device designed for pain management using infrared light therapy.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Beamer Painlow Infrared Light Treatment System Ref K052307
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beamline Corporation have in the registry?
The registry currently lists 1 device for Beamline Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beamline Corporation's devices?
Among its 1 most recently registered device, Beamline Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Beamline Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Beamline Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beamline Corporation in the registry?
The most recently registered devices listed for Beamline Corporation include BEAMER PAINLOW INFRARED LIGHT TREATMENT SYSTEM.