FDA applicant

Sporicidin Intl.

Rockville, MD8 decisions1983–20000 recalls

FDA records 8 decisions for Sporicidin Intl. (Rockville, MD) from 1983 to 2000: 8 510(k) clearances. Most are in product codes LRJ (Disinfectant, Medical Devices) and MED (Sterilant, Medical Devices). 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 Sporicidin Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sporicidin Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Sporicidin Intl.

Which product codes does it file in?

What has FDA decided for it lately?