FDA applicant
Everyway Medical Instrument Co., Ltd.
FDA records 2 decisions for Everyway Medical Instrument Co., Ltd. (Shenkeng District, New Taipei City, CN) in 2017: 2 510(k) clearances. Most are in product codes KPI (Stimulator, Electrical, Non-Implantable, For…) and NGX (Stimulator, Muscle, Powered, For Muscle…). 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 Everyway Medical Instrument Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Everyway Medical Instrument 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) ReportOther applicant names beginning “Everyway”
FDA records each applicant name separately; these may or may not be the same firm.