FDA applicant
Home Care Technology Co., Ltd.
FDA records 4 decisions for Home Care Technology Co., Ltd. (Columbus, OH) in 2003: 4 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GXY (Electrode, Cutaneous). 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 Home Care Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Home Care Technology Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Home Care Technology Co., Ltd.’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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