Cleveland Clinic
Country not established
- Devices
- 1
What Cleveland Clinic makes
The Cleveland Clinic manufactures the Glenoid Intelligent Reusable Instrument System (Glenoid IRIS), a reusable orthopedic instrument designed for shoulder surgery, specifically for glenoid preparation in reverse shoulder arthroplasty procedures.
The Glenoid IRIS is classified as a Class II medical device under FDA regulations and is listed in the FDA 510(k) database. The company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cleveland Clinic have in the registry?
The registry currently lists 1 device for Cleveland Clinic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cleveland Clinic's devices?
Among its 1 most recently registered device, Cleveland Clinic has devices listed in FDA 510(k) (1 device).
What risk classes do Cleveland Clinic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cleveland Clinic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cleveland Clinic in the registry?
The most recently registered devices listed for Cleveland Clinic include GLENOID INTELLIGENT REUSABLE INSTRUMENT SYSTEM (GLENOID IRIS).