Surgeon Design
Country not established
- Devices
- 1
What Surgeon Design makes
Surgeon Design manufactures the OCUSYSTEM IIE, a surgical device designed for ophthalmic procedures, specifically intended for intraocular applications.
The OCUSYSTEM IIE is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Ocusystem Iie Ref K926381
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgeon Design have in the registry?
The registry currently lists 1 device for Surgeon Design. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgeon Design's devices?
Among its 1 most recently registered device, Surgeon Design has devices listed in FDA 510(k) (1 device).
What risk classes do Surgeon Design's devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgeon Design's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgeon Design in the registry?
The most recently registered devices listed for Surgeon Design include OCUSYSTEM IIE.