FDA applicant

Health Improvement Assoc.

Freeland, MI4 decisions1977–19950 recalls

FDA records 4 decisions for Health Improvement Assoc. (Freeland, MI) from 1977 to 1995: 4 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and IMB (Cabinet, Moist Steam). 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 Improvement Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Health Improvement Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Health Improvement Assoc.’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

Health Improvement Assoc.

Which product codes does it file in?

What has FDA decided for it lately?