Iris Surgical, LLC
Country not established
- Devices
- 1
What Iris Surgical, LLC makes
Iris Surgical, LLC manufactures the Kilejian Circumcisor, a surgical device designed for the circumcision procedure in clinical settings.
The Kilejian Circumcisor is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Kilejian Circumcisor Ref K010867
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iris Surgical, LLC have in the registry?
The registry currently lists 1 device for Iris Surgical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iris Surgical, LLC's devices?
Among its 1 most recently registered device, Iris Surgical, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Iris Surgical, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Iris Surgical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iris Surgical, LLC in the registry?
The most recently registered devices listed for Iris Surgical, LLC include KILEJIAN CIRCUMCISOR.