FDA applicant

Flexodent Corp.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Flexodent Corp. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code EKO (Denture Preformed (Partially Prefabricated…). 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 Flexodent Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Flexodent Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Flexodent Corp.

Which product codes does it file in?

What has FDA decided for it lately?