Medical Device Manufacturer · US , Flagstaff , AZ

I-See Vision Technology, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2009

Total

Cleared

Denied

I-See Vision Technology, Inc. has 4 FDA 510(k) cleared medical devices. Based in Flagstaff, US.

Historical record: 4 cleared submissions from 2009 to 2015. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by I-See Vision Technology, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.

I-See Vision Technology, Inc. is one of 25971 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - I-See Vision Technology, Inc.

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 21, 2026