FDA applicant

R. Kent Richards, Inc.

Pl. Grove, UT12 decisions1985–19870 recalls

FDA records 12 decisions for R. Kent Richards, Inc. (Pl. Grove, UT) from 1985 to 1987: 12 510(k) clearances. Most are in product codes JSI (Culture Media, Selective And Differential) and JSJ (Culture Media, Selective And Non-Differential). 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, microbiology panel, where it files most

How often FDA has decided R. Kent Richards, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for R. Kent Richards, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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R. Kent Richards, Inc.

Which product codes does it file in?

What has FDA decided for it lately?