FDA applicant

Arnold & Sons

Walker, MI1 decision1983–19830 recalls

FDA records 1 decision for Arnold & Sons (Walker, MI) in 1983: 1 510(k) clearance. All are in product code FLE (Sterilizer, Steam). 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 Arnold & Sons’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arnold & Sons since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Arnold”

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

Arnold & Richter Cine Technik 2 Arnold Technologies 2 Arnold & Porter For G.E. Co. 1 Arnold Tuber Industries 1

Arnold & Sons

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arnold”