FDA applicant

Preventive Medicine Institute

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Preventive Medicine Institute (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code FCG (Biopsy Needle). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Preventive Medicine Institute’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Preventive Medicine Institute since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Preventive Medicine Institute’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

Other applicant names beginning “Preventive”

FDA records each applicant name separately; these may or may not be the same firm.

Preventive Diagnostics Corp. 18 Preventive Care, Inc. 3 Preventive Technologies, Inc. 3

Preventive Medicine Institute

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Preventive”