FDA applicant

The Gillette Company

Mchenry, IL3 decisions1979–19800 recalls

FDA records 3 decisions for The Gillette Company (Mchenry, IL) from 1979 to 1980: 3 510(k) clearances. Most are in product codes IRT (Pad, Heating, Powered) and ILJ (Bath, Hydro-Massage). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for The Gillette Company since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “The”

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

Gillette Children'S Specialty Healthcare 1

The Gillette Company

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”