FDA applicant

E.M. Adams

Mchenry, IL23 decisions1978–19970 recalls

FDA records 23 decisions for E.M. Adams (Mchenry, IL) from 1978 to 1997: 23 510(k) clearances. Most are in product codes FSM (Tray, Surgical, Instrument) and EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.

FDA’s records also spell it “E.M. Adams Co., Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided E.M. Adams’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E.M. Adams since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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E.M. Adams

Which product codes does it file in?

What has FDA decided for it lately?