FDA applicant

H & M Douglas Enterprises, Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for H & M Douglas Enterprises, Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code FTZ (Locator, Magnetic). 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, ophthalmic panel, where it files most

How often FDA has decided H & M Douglas Enterprises, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for H & M Douglas Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — H & M Douglas Enterprises, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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H & M Douglas Enterprises, Inc.

Which product codes does it file in?

What has FDA decided for it lately?