American Spine Center, Ltd.
Country not established
- Devices
- 1
What American Spine Center, Ltd. makes
American Spine Center, Ltd. manufactures the CLINI-LASE laser systems, including base models and variants such as the CL-BASE, CL-2000, and CL-155, designed for spinal and orthopedic procedures.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Spine Center, Ltd. have in the registry?
The registry currently lists 1 device for American Spine Center, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Spine Center, Ltd.'s devices?
Among its 1 most recently registered device, American Spine Center, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do American Spine Center, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Spine Center, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Spine Center, Ltd. in the registry?
The most recently registered devices listed for American Spine Center, Ltd. include CLINI-LASE SYSTEM, MODELS CL-BASE, CL-2000, CL-1200, CL-500, CL-300, CL-275, CL-155, CL-55, CLP-BASE, CLP-275, CLP-55..