FDA applicant

Medprobe Laboratories

Mchenry, IL4 decisions1982–19830 recalls

FDA records 4 decisions for Medprobe Laboratories (Mchenry, IL) from 1982 to 1983: 4 510(k) clearances. All are in product code FMK (Single Use Only Blood Lancet With An Integral…). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Medprobe Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medprobe Laboratories’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Medprobe Laboratories

Which product codes does it file in?

What has FDA decided for it lately?