FDA applicant
Di-Equi Dental Products
FDA records 2 decisions for Di-Equi Dental Products (Mchenry, IL) in 1984: 2 510(k) clearances. All are in product code EHY (Tray, Impression, Preformed). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Di-Equi Dental Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Di-Equi Dental Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Di-Equi Dental Products’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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