Medical Device Manufacturer · KR , Seoul

INTEROJO, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2015

Total

Cleared

Denied

INTEROJO, Inc. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Latest FDA clearance: May 2026. Active since 2015. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by INTEROJO, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Eyereg Consulting, Inc. and Andre Vision and Device Research.

INTEROJO, Inc. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - INTEROJO, Inc.

4 devices

1-4 of 4

Data Source

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

Last updated: Jun 05, 2026