FDA applicant

Ocg Technology, Inc.

Farmingdale, NY3 decisions1981–19870 recalls

FDA records 3 decisions for Ocg Technology, Inc. (Farmingdale, NY) from 1981 to 1987: 3 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) and DSI (Detector And Alarm, Arrhythmia). 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, cardiovascular panel, where it files most

How often FDA has decided Ocg Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ocg Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ocg Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?