FDA applicant

Alexander Mfg. Co.

Mason City, IA39 decisions1997–19980 recalls

FDA records 39 decisions for Alexander Mfg. Co. (Mason City, IA) from 1997 to 1998: 39 510(k) clearances. Most are in product codes MRZ (Accessories, Pump, Infusion) and DQA (Oximeter). Its devices cite 21 predicates, 0 of them its own earlier devices. 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, general hospital panel, where it files most

How often FDA has decided Alexander Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alexander Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Alexander Mfg. Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Alexander”

FDA records each applicant name separately; these may or may not be the same firm.

Alexander Thomas, Inc. 1 Alexander Medical, Inc. 1

Alexander Mfg. Co.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Alexander”