FDA applicant
Mytech Technology Co., Ltd.
FDA records 4 decisions for Mytech Technology Co., Ltd. (Hsin-Chu City, TW) from 2003 to 2006: 4 510(k) clearances. All are in product code DXN (System, Measurement, Blood-Pressure…). Its devices cite 2 predicates, 2 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 Mytech Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Mytech Technology Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Mytech 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.
See the 510(k) ReportOther applicant names beginning “Mytech”
FDA records each applicant name separately; these may or may not be the same firm.