510(k) Report

FDA applicant

Dentalpure Corp.

St. Paul, MN1 decision1997–19970 recalls

FDA records 1 decision for Dentalpure Corp. (St. Paul, MN) in 1997: 1 510(k) clearance. All are in product code EIA (Unit, Operative Dental). 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 Dentalpure Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dentalpure Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dentalpure 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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