FDA applicant

Dms Products, Inc.

Flemington, NJ6 decisions1986–19890 recalls

FDA records 6 decisions for Dms Products, Inc. (Flemington, NJ) from 1986 to 1989: 6 510(k) clearances. Most are in product codes JSS (Kit, Identification, Enterobacteriaceae) and JST (Kit, Fastidious Organisms). 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 Dms Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dms Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dms Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?