FDA applicant
Vacudent Sales Corp.
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
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.
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