FDA applicant

Tempo Technology, Inc.

Columbia City, IN3 decisions1990–19960 recalls

FDA records 3 decisions for Tempo Technology, Inc. (Columbia City, IN) from 1990 to 1996: 3 510(k) clearances. Most are in product codes OXO (Image-Intensified Fluoroscopic X-Ray System…) and IMD (Pack, Hot Or Cold, Disposable). 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, radiology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Tempo Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?