FDA applicant

Optomotor Laboratories

D-79104 Freiburg, DE1 decision1999–19990 recalls

FDA records 1 decision for Optomotor Laboratories (D-79104 Freiburg, DE) in 1999: 1 510(k) clearance. All are in product code GWN (Nystagmograph). 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, neurology panel, where it files most

How often FDA has decided Optomotor Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Optomotor Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Optomotor Laboratories

Which product codes does it file in?

What has FDA decided for it lately?