Medical Device Manufacturer · US , Plano , TX

Elekon Industries U.S.A., Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2004

Total

Cleared

Denied

Elekon Industries U.S.A., Inc. has 6 FDA 510(k) cleared medical devices. Based in Plano, US.

Historical record: 6 cleared submissions from 2004 to 2004. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Elekon Industries U.S.A., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Elekon Industries U.S.A., Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 27, 2026