FDA applicant

Eaton Medical Corp.

Memphis, TN5 decisions1984–19930 recalls

FDA records 5 decisions for Eaton Medical Corp. (Memphis, TN) from 1984 to 1993: 5 510(k) clearances. Most are in product codes LYL (Accessories, Solution, Ultrasonic Cleaners For…) and HPX (Lens, Contact (Polymethylmethacrylate)). 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 Eaton Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eaton Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Eaton”

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

Eaton Medical Group 15

Eaton Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Eaton”