510(k) Report

FDA applicant

Wat Medical Technology (Ningbo) Co., Ltd.

Ningbo, CN2 decisions2018–20180 recalls

FDA records 2 decisions for Wat Medical Technology (Ningbo) Co., Ltd. (Ningbo, CN) in 2018: 2 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and PCC (Stimulator, Nerve, Electrical, Transcutaneous…). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 Wat Medical Technology (Ningbo) Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2018

2018: 2
2018high 2 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Wat Medical Technology (Ningbo) Co., Ltd. by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wat Medical Technology (Ningbo) Co.…’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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