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) Regulatory Record - Propper Manufacturing Co., Inc.

7 devices

1-7 of 7