Retina Tester
Country not established
- Devices
- 1
What Retina Tester makes
The company manufactures the Retina Tester, a diagnostic device used for evaluating retinal health and detecting conditions such as macular degeneration, diabetic retinopathy, or retinal detachment through imaging and analysis.
The Retina Tester is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Retina Tester Ref K914393
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Retina Tester have in the registry?
The registry currently lists 1 device for Retina Tester. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retina Tester's devices?
Among its 1 most recently registered device, Retina Tester has devices listed in FDA 510(k) (1 device).
What risk classes do Retina Tester's devices fall under?
Among its 1 most recently registered device, the classes recorded for Retina Tester's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retina Tester in the registry?
The most recently registered devices listed for Retina Tester include RETINA TESTER.