FDA applicant

Precision Dynamics Corp.

Mchenry, IL26 decisions1977–20160 recalls

FDA records 26 decisions for Precision Dynamics Corp. (Mchenry, IL) from 1977 to 2016: 26 510(k) clearances. Most are in product codes JTW (System, Transport, Aerobic) and JSM (Culture Media, Non-Propagating Transport). Its devices cite 5 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Precision Dynamics Corporation”.

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 Precision Dynamics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2007high 1 (2016) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Precision Dynamics Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Precision Dynamics Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?