FDA applicant
Cavity Free Kids, Inc.
FDA records 1 decision for Cavity Free Kids, Inc. (St. Paul, MN) in 1997: 1 510(k) clearance. All are in product code FMQ (Restraint, Protective). 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 Cavity Free Kids, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cavity Free Kids, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cavity Free Kids, Inc.’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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