Medical Device Manufacturer · US , Long Island , NY

Propper Manufacturing Co., Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2014

Total

Cleared

Denied

Propper Manufacturing Co., Inc. has 7 FDA 510(k) cleared medical devices. Based in Long Island, US.

Latest FDA clearance: Oct 2025. Active since 2014. Primary specialty: General Hospital.

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

FDA 510(k) cleared devices by Propper Manufacturing Co., Inc.

7 devices

1-7 of 7