510(k) Report

FDA applicant

Shenzhen As-Tec Technology Co., Ltd.

Shenzhen, CN1 decision2015–20150 recalls

FDA records 1 decision for Shenzhen As-Tec Technology Co., Ltd. (Shenzhen, CN) in 2015: 1 510(k) clearance. All are in product code NUH (Stimulator, Nerve, Transcutaneous…). 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, neurology panel, where it files most

How often FDA has decided Shenzhen As-Tec Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Shenzhen As-Tec Technology Co., Ltd. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NUHStimulator, Nerve, Transcutaneous, Over-The-Counter1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K143268Tens and Powered Muscle StimulatorShenzhen As-Tec Technology Co., Ltd. · 20153cite it

What has FDA decided for it lately?

  • K143268Tens and Powered Muscle StimulatorShenzhen As-Tec Technology Co., Ltd. · 2015

The one decision as Shenzhen As-Tec Technology Co., Ltd. →