FDA applicant

Cavitron Corp.

Mchenry, IL32 decisions1976–19810 recalls

FDA records 32 decisions for Cavitron Corp. (Mchenry, IL) from 1976 to 1981: 32 510(k) clearances. Most are in product codes CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase) and EHL (Point, Abrasive). 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 Cavitron Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cavitron Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Cavitron”

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

Cavitron Surgical Systems 1

Cavitron Corp.

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 “Cavitron”