FDA applicant
Kunshan Aoshida Electric Technology Co., Ltd.
FDA records 1 decision for Kunshan Aoshida Electric Technology Co., Ltd. (Kunshan, CN) in 2017: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). Its devices cite 1 predicate, 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 Kunshan Aoshida Electric Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Kunshan Aoshida Electric Technology…’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) ReportOther applicant names beginning “Kunshan”
FDA records each applicant name separately; these may or may not be the same firm.