510(k) Report

FDA applicant

Nai Technology Products

Upland, CA1 decision2004–20040 recalls

FDA records 1 decision for Nai Technology Products (Upland, CA) in 2004: 1 510(k) clearance. All are in product code LMA (Digitizer, Image, Radiological). 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, radiology panel, where it files most

How often FDA has decided Nai Technology Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nai Technology Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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