FDA applicant

Ciba-Geigy Corp.

Walker, MI2 decisions1983–20010 recalls

FDA records 2 decisions for Ciba-Geigy Corp. (Walker, MI) from 1983 to 2001: 2 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and MVN (Lens, Contact, (Disposable)). 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 Ciba-Geigy Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ciba-Geigy Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ciba-Geigy 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 “Ciba-Geigy”

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

Ciba Corning Diagnostics Corp. 125 Ciba Vision Corporation 56 Ciba Vision Care 4 Ciba Vision Johns Creek Mfg. 1

Ciba-Geigy Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ciba-Geigy”