FDA applicant
Wat Medical Technology (Ningbo) Co., Ltd.
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
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
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2018.
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.
See the 510(k) Report