510(k) Report

FDA applicant

The Safegard Protection Corp.

Wailuku, HI1 decision1989–19890 recalls

FDA records 1 decision for The Safegard Protection Corp. (Wailuku, HI) in 1989: 1 510(k) clearance. All are in product code HIS (Condom). 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 The Safegard Protection Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Safegard Protection Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Safegard Protection 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 “The”

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