FDA applicant

Paragon Diagnostics, Inc.

Mchenry, IL7 decisions1984–19840 recalls

FDA records 7 decisions for Paragon Diagnostics, Inc. (Mchenry, IL) in 1984: 7 510(k) clearances. Most are in product codes KHQ (Radioassay, Triiodothyronine Uptake) and JZT (Fluorometer). 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, clinical toxicology panel, where it files most

How often FDA has decided Paragon Diagnostics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paragon Diagnostics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Paragon Diagnostics, 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 “Paragon”

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

Paragon 28, Inc. 61 Paragon Vision Sciences 16 Paragon Trade Brands, Inc. 14 Paragon Medical 5 Paragon Implant Mfg., LLC 5 Paragon Optical Co. 2 Paragon Medical and Scientific, Inc. 1 Paragon Bioteck, Inc. 1

Paragon Diagnostics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paragon”