Medical Device Manufacturer · US , New York , NY

Paieon, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2004

Total

Cleared

Denied

Paieon, Inc. has 8 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 8 cleared submissions from 2004 to 2012. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Paieon, Inc.

8 devices

1-8 of 8

Data Source

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

Last updated: Apr 27, 2026