Oculon Corp.
Country not established
- Devices
- 1
What Oculon Corp. makes
Oculon Corp. manufactures the OPACITRAC, a device designed for measuring intraocular lens opacity and assessing posterior capsule opacification in patients post-cataract surgery.
The OPACITRAC 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
Opacitrac Ref K915356
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oculon Corp. have in the registry?
The registry currently lists 1 device for Oculon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oculon Corp.'s devices?
Among its 1 most recently registered device, Oculon Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Oculon Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oculon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oculon Corp. in the registry?
The most recently registered devices listed for Oculon Corp. include OPACITRAC.