Ocular Systems, Inc.
Country not established
- Devices
- 1
What Ocular Systems, Inc. makes
Ocular Systems, Inc. manufactures the Endosert, a device designed for intraocular injection procedures, facilitating precise delivery of medications or substances into the eye.
The Endosert is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Endoserter Ref K090626
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ocular Systems, Inc. have in the registry?
The registry currently lists 1 device for Ocular Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ocular Systems, Inc.'s devices?
Among its 1 most recently registered device, Ocular Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ocular Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ocular Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ocular Systems, Inc. in the registry?
The most recently registered devices listed for Ocular Systems, Inc. include ENDOSERTER.