FDA applicant

Vistech Consultants, Inc.

Dayton, OH7 decisions1984–19880 recalls

FDA records 7 decisions for Vistech Consultants, Inc. (Dayton, OH) from 1984 to 1988: 7 510(k) clearances. All are in product code 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 Vistech Consultants, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vistech Consultants, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vistech Consultants, Inc.

Which product codes does it file in?

What has FDA decided for it lately?