FDA applicant

Calgon Vestal Div.

St. Louis, MO19 decisions1989–19940 recalls

FDA records 19 decisions for Calgon Vestal Div. (St. Louis, MO) from 1989 to 1994: 19 510(k) clearances. Most are in product codes LRJ (Disinfectant, Medical Devices) and FLG (Cleaner, Ultrasonic, Medical Instrument). 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, general hospital panel, where it files most

How often FDA has decided Calgon Vestal Div.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Calgon Vestal Div. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Calgon”

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

Calgon Corp. 5

Calgon Vestal Div.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Calgon”