510(k) Report

FDA applicant

Mini Floss

Tempe, AZ1 decision1985–19850 recalls

FDA records 1 decision for Mini Floss (Tempe, AZ) in 1985: 1 510(k) clearance. All are in product code JES (Floss, 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 Mini Floss’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mini Floss since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mini”

FDA records each applicant name separately; these may or may not be the same firm.