Medical Device Manufacturer · US , Bridgeport , CT

Remington Products Company, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1989

Total

Cleared

Denied

Remington Products Company, LLC has 3 FDA 510(k) cleared medical devices. Based in Bridgeport, US.

Historical record: 3 cleared submissions from 1989 to 2001. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Remington Products Company, LLC Filter by specialty or product code using the sidebar.

3 devices

1–3 of 3

Data Source

FDA 510(k) public files . 174,402 total devices indexed.