510(k) Report

FDA applicant

FDA Agents

Tampa, FL1 decision2005–20050 recalls

FDA records 1 decision for FDA Agents (Tampa, FL) in 2005: 1 510(k) clearance. All are in product code DYW (Bracket, Plastic, Orthodontic). 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 FDA Agents’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for FDA Agents since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like FDA Agents’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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