Intraoptics, Inc.
Country not established
- Devices
- 1
What Intraoptics, Inc. makes
Intraoptics, Inc. manufactures the OPACITY LENSMETER 701, a device used to measure intraocular lens opacity in ophthalmic applications.
The OPACITY LENSMETER 701 is classified as a Class II medical device and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
Opacity Lensmeter 701 Ref K874355
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intraoptics, Inc. have in the registry?
The registry currently lists 1 device for Intraoptics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intraoptics, Inc.'s devices?
Among its 1 most recently registered device, Intraoptics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intraoptics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intraoptics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intraoptics, Inc. in the registry?
The most recently registered devices listed for Intraoptics, Inc. include OPACITY LENSMETER 701.