510(k) Report

FDA applicant

Health Development Corp.

Mchenry, IL5 decisions1980–19830 recalls

FDA records 5 decisions for Health Development Corp. (Mchenry, IL) from 1980 to 1983: 5 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and HIS (Condom). 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 Health Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Health Development Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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