510(k) Report

FDA applicant

Tang Products

Aurora, CO1 decision1985–19850 recalls

FDA records 1 decision for Tang Products (Aurora, CO) in 1985: 1 510(k) clearance. All are in product code KMT (Tray, Fluoride, Disposable). 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 Tang Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tang Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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