510(k) Report

FDA applicant

Anhui Jinjianqiao Med-Tech Co,., Ltd.

Shenzhen, Guangdong, CN1 decision2013–20130 recalls

FDA records 1 decision for Anhui Jinjianqiao Med-Tech Co,., Ltd. (Shenzhen, Guangdong, CN) in 2013: 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 Anhui Jinjianqiao Med-Tech Co,., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Anhui Jinjianqiao Med-Tech Co,., Ltd. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Anhui Jinjianqiao Med-Tech Co,., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

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

What has FDA decided for it lately?

  • K130150TCM MassagerAnhui Jinjianqiao Med-Tech Co,., Ltd. · 2013

The one decision as Anhui Jinjianqiao Med-Tech Co,., Ltd. →