FDA applicant

Kinetix

Mchenry, IL4 decisions1983–19840 recalls

FDA records 4 decisions for Kinetix (Mchenry, IL) from 1983 to 1984: 4 510(k) clearances. Most are in product codes BYP (Mouthpiece, Breathing) and BZG (Spirometer, Diagnostic). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Kinetix since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kinetix”

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

Kinetix Instruments 1

Kinetix

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kinetix”