Inneroptic Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Inneroptic Technology, Inc. makes
Inneroptic Technology, Inc. manufactures the AIM, a diagnostic imaging device for ophthalmic applications, and the INVISION SYSTEM, a surgical tool used in cataract procedures to perform laser-assisted corneal incisions and lens fragmentation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Aim Ref K121479
Regimes: 510(k) Registry: 510(k)Invision System Ref K083728
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inneroptic Technology, Inc. have in the registry?
The registry currently lists 2 devices for Inneroptic Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inneroptic Technology, Inc.'s devices?
Among its 2 most recently registered devices, Inneroptic Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Inneroptic Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Inneroptic Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inneroptic Technology, Inc. in the registry?
The most recently registered devices listed for Inneroptic Technology, Inc. include AIM and INVISION SYSTEM.