FDA applicant

Teca, Inc.

Pleasantiville, NY29 decisions1976–19960 recalls

FDA records 29 decisions for Teca, Inc. (Pleasantiville, NY) from 1976 to 1996: 29 510(k) clearances. Most are in product codes GWQ (Full-Montage Standard Electroencephalograph) and GWE (Stimulator, Photic, Evoked Response). 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 Teca, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teca, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Teca, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?