FDA applicant

Neoprobe Corp.

Dublin, OH6 decisions1986–20050 recalls

FDA records 6 decisions for Neoprobe Corp. (Dublin, OH) from 1986 to 2005: 6 510(k) clearances. Most are in product codes IZD (Probe, Uptake, Nuclear) and DPW (Flowmeter, Blood, Cardiovascular). Its devices cite 8 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Neoprobe Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neoprobe Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Neoprobe Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Neoprobe Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?