FDA applicant

Dayton Mfg. Co.

Tampa, FL2 decisions1987–19870 recalls

FDA records 2 decisions for Dayton Mfg. Co. (Tampa, FL) in 1987: 2 510(k) clearances. Most are in product codes KYE (Inserter/Remover Contact Lens) and LRX (Case, Contact Lens). 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, ophthalmic panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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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 Water Systems 3

Dayton Mfg. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dayton”