510(k) Report

FDA applicant

Fred M. Davis

Walker, MI1 decision1983–19830 recalls

FDA records 1 decision for Fred M. Davis (Walker, MI) in 1983: 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 Fred M. Davis’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fred M. Davis since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Fred”

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