Medical Device Manufacturer · US , Columbus , OH

Neoprobe Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1986

Total

Cleared

Denied

Neoprobe Corp. has 6 FDA 510(k) cleared medical devices. Based in Columbus, US.

Historical record: 6 cleared submissions from 1986 to 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Neoprobe Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Neoprobe Corp.

6 devices

1-6 of 6

Data Source

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

Last updated: Apr 27, 2026