FDA applicant
Shenzhen Jingkehui Electronic Co.., Ltd.
FDA records 3 decisions for Shenzhen Jingkehui Electronic Co.., Ltd. (Mountain View, CA) from 2013 to 2015: 3 510(k) clearances. All are in product code NUH (Stimulator, Nerve, Transcutaneous…). Its devices cite 3 predicates, 1 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 Shenzhen Jingkehui Electronic Co.., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2015
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2013.
Planning a device like Shenzhen Jingkehui Electronic 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