FDA applicant

M-Pact Corp.

Eudora, KS1 decision1999–19990 recalls

FDA records 1 decision for M-Pact Corp. (Eudora, KS) in 1999: 1 510(k) clearance. All are in product code HOZ (Sponge, Ophthalmic). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for M-Pact Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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M-Pact Corp.

Which product codes does it file in?

What has FDA decided for it lately?