FDA applicant

Stereo Optical Co., Inc.

Chicago, IL5 decisions1984–19930 recalls

FDA records 5 decisions for Stereo Optical Co., Inc. (Chicago, IL) from 1984 to 1993: 5 510(k) clearances. Most are in product codes HKO (Refractometer, Ophthalmic) and HOX (Chart, Visual Acuity). 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 Stereo Optical Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stereo Optical Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Stereo Optical Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?