FDA applicant
E-Woo Technology
FDA records 8 decisions for E-Woo Technology (Houston, TX) from 2007 to 2010: 8 510(k) clearances. Most are in product codes JAK (System, X-Ray, Tomography, Computed) and OAS (X-Ray, Tomography, Computed, Dental). Its devices cite 11 predicates, 3 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “E-Woo Technology Co., Ltd.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided E-Woo Technology’s devices, and how often a recall has named them.
FDA decisions per year
1in 2010
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like E-Woo 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) Report