Medical Device Manufacturer · US , Chicago , IL

The Lagado Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2004

Total

Cleared

Denied

The Lagado Corp. has 5 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 5 cleared submissions from 2004 to 2013. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by The Lagado Corp. Filter by specialty or product code using the sidebar.

1 device has linked clinical trial registered on ClinicalTrials.gov.

The Lagado Corp. is one of 21672 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - The Lagado Corp.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 17, 2026