FDA applicant

Mem, Inc.

Mchenry, IL2 decisions1983–19840 recalls

FDA records 2 decisions for Mem, Inc. (Mchenry, IL) from 1983 to 1984: 2 510(k) clearances. All are in product code LAE (High Pressure Liquid Chromatography, Codeine). 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, clinical toxicology panel, where it files most

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

FDA decisions per year

No FDA decision for Mem, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mem, Inc.

Which product codes does it file in?

What has FDA decided for it lately?