FDA applicant

Kao Corp.

Tokyo 103 Japan, JP9 decisions1984–19890 recalls

FDA records 9 decisions for Kao Corp. (Tokyo 103 Japan, JP) from 1984 to 1989: 9 510(k) clearances. All are in product code HHD (Pad, Menstrual, Unscented). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Kao Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Kao Corp.

Which product codes does it file in?

What has FDA decided for it lately?