FDA applicant
Tung FU Electric Co., Ltd.
FDA records 2 decisions for Tung FU Electric Co., Ltd. (San Chung, Taipei, TW) from 2005 to 2006: 2 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Tung FU Electric Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Tung FU Electric Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Tung FU Electric 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 “Tung”
FDA records each applicant name separately; these may or may not be the same firm.