FDA applicant

Columbus Dental Mfg. Co.

St. Louis, MO11 decisions1983–19880 recalls

FDA records 11 decisions for Columbus Dental Mfg. Co. (St. Louis, MO) from 1983 to 1988: 11 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and EGD (Wax, Dental, Intraoral). 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, dental panel, where it files most

How often FDA has decided Columbus Dental Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Columbus Dental Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Columbus Dental Mfg. Co. 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 Instruments Intl. Corp. 5 Columbus Mckinnon Corp. 1

Columbus Dental Mfg. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Columbus”