FDA applicant

Kronus Market Development Associates, Inc.

Boise, ID11 decisions2003–20140 recalls

FDA records 11 decisions for Kronus Market Development Associates, Inc. (Boise, ID) from 2003 to 2014: 10 510(k) clearances and 1 De Novo grant. Most are in product codes NST (Autoantibodies, Acetylcholine Receptor…) and NWG (Autoantibodies, Glutamic Acid Decarboxylase…). 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, immunology panel, where it files most

How often FDA has decided Kronus Market Development Associates, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2007high 3 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kronus”

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

Kronus, Inc. 9

Kronus Market Development Associates, Inc.

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 “Kronus”