510(k) Report

FDA applicant

Ipco Corp.

Mchenry, IL23 decisions1976–19870 recalls

FDA records 23 decisions for Ipco Corp. (Mchenry, IL) from 1976 to 1987: 23 510(k) clearances. Most are in product codes EYQ (Garment, Protective, For Incontinence) and 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Ipco Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ipco Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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