Sunning Corp.
Country not established
- Devices
- 1
What Sunning Corp. makes
Sunning Corp. manufactures the SUNSCOPE 100, a medical imaging device designed for diagnostic purposes in ophthalmology, likely used for retinal imaging or fundus photography.
The SUNSCOPE 100 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Sunscope 100 Ref K931941
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sunning Corp. have in the registry?
The registry currently lists 1 device for Sunning Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sunning Corp.'s devices?
Among its 1 most recently registered device, Sunning Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Sunning Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sunning Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sunning Corp. in the registry?
The most recently registered devices listed for Sunning Corp. include SUNSCOPE 100.