FDA applicant

Epson America, Inc.

Los Angeles, CA3 decisions1985–19930 recalls

FDA records 3 decisions for Epson America, Inc. (Los Angeles, CA) from 1985 to 1993: 3 510(k) clearances. All are in product code FLL (Continuous Measurement Thermometer). 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 Epson America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Epson America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Epson”

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

Epson EL Paso, Inc. 1

Epson America, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Epson”