FDA applicant

Penox Technologies, Inc.

Pittston, PA10 decisions1985–19870 recalls

FDA records 10 decisions for Penox Technologies, Inc. (Pittston, PA) from 1985 to 1987: 10 510(k) clearances. Most are in product codes CAM (Yoke Assembly, Medical Gas) and INO (Chair, Positioning, Electric). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Penox Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Penox Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?