FDA applicant

Contraves Goerz Corp.

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Contraves Goerz Corp. (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code LXV (Apparatus, Vestibular Analysis). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

No FDA decision for Contraves Goerz Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Contraves Goerz 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 “Contraves”

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

Contraves Medical Instruments, Inc. 3 Contraves 1

Contraves Goerz Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Contraves”