FDA applicant

Seca Corp.

Mchenry, IL5 decisions1982–20200 recalls

FDA records 5 decisions for Seca Corp. (Mchenry, IL) from 1982 to 2020: 5 510(k) clearances. Most are in product codes FRW (Scale, Patient) and MNW (Analyzer, Body Composition). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Seca GmbH & Co. KG”.

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

FIG. A — Illustration, general hospital panel, where it files most

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

FDA decisions per year

1in 2020

2007high 1 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Seca Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?