FDA applicant

Columbus Instruments Intl. Corp.

Columbus, OH5 decisions1977–19900 recalls

FDA records 5 decisions for Columbus Instruments Intl. Corp. (Columbus, OH) from 1977 to 1990: 5 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) and GYD (Transducer, Tremor). 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 Columbus Instruments Intl. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Columbus Instruments Intl. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Columbus”

FDA records each applicant name separately; these may or may not be the same firm.

Columbus Dental Mfg. Co. 11 Columbus Mckinnon Corp. 1

Columbus Instruments Intl. Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Columbus”