Medical Device Manufacturer · US , New York , NY

Segi Hearing Aid Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1996

Total

Cleared

Denied

Segi Hearing Aid Co. has 1 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Segi Hearing Aid Co. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Segi Hearing Aid Co.

1 devices

1-1 of 1

Data Source

Sourced from the FDA 510(k) public files . 174,477 total devices indexed.

Last updated: Mar 22, 2026