Medical Device Manufacturer · US , Littleton , CO

Biomaterials Korea, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

Biomaterials Korea, Inc. has 5 FDA 510(k) cleared medical devices. Based in Littleton, US.

Last cleared in 2023. Active since 2007. Primary specialty: Dental.

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

510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.

Biomaterials Korea, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biomaterials Korea, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 15, 2026