510(k) Report

FDA applicant

Vacudent Sales Corp.

Mchenry, IL4 decisions1978–19800 recalls

FDA records 4 decisions for Vacudent Sales Corp. (Mchenry, IL) from 1978 to 1980: 4 510(k) clearances. Most are in product codes EHP (Clasp, Preformed) and 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 Vacudent Sales Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vacudent Sales Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report