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.

Neoprobe Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neoprobe Corp.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026