Cmsi
Country not established
- Devices
- 3
What Cmsi makes
Cmsi manufactures surgical cutting tools, including the CMS FAST CUT, CMS DIAMOND, and CMS WIRE PASS, designed for precise tissue separation. Their product line also includes bilateral collimators for targeted medical imaging applications and tomographic software programs for advanced imaging analysis.
The company’s devices are classified under FDA categories Class I and Class II, with regulatory submissions supported through the 510(k) pathway. These products are listed under U.S. FDA regulations, and the manufacturer operates from the United States.
Catalogue
Cms Fast Cut, Cms Diamond And Cms Wire Pass Ref K893499
Regimes: 510(k) Registry: 510(k)Tomographic Programs Ref K790169
Regimes: 510(k) Registry: 510(k)Collimator, Bilaterial Ref K790168
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cmsi have in the registry?
The registry currently lists 3 devices for Cmsi. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cmsi's devices?
Among its 3 most recently registered devices, Cmsi has devices listed in FDA 510(k) (3 devices).
What risk classes do Cmsi's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cmsi's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cmsi in the registry?
The most recently registered devices listed for Cmsi include CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS, TOMOGRAPHIC PROGRAMS and COLLIMATOR, BILATERIAL.