Medical Device Manufacturer · US , Walker , MI

The Richmond Light Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1981

Total

Cleared

Denied

The Richmond Light Co. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1981 to 2005. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - The Richmond Light Co.

2 devices

1-2 of 2

Data Source

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

Last updated: Apr 28, 2026