FDA applicant

Dayton Water Systems

Dayton, OH3 decisions1995–20020 recalls

FDA records 3 decisions for Dayton Water Systems (Dayton, OH) from 1995 to 2002: 3 510(k) clearances. All are in product code FIP (Subsystem, Water Purification). Its devices cite 1 predicate, 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, gastroenterology and urology panel, where it files most

How often FDA has decided Dayton Water Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dayton Water Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dayton Water Systems’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 “Dayton”

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

Dayton Mfg. Co. 2

Dayton Water Systems

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Dayton”