FDA applicant
Wuxi Medical Instrument Factory
FDA records 1 decision for Wuxi Medical Instrument Factory (Shanghai, CN) in 2011: 1 510(k) clearance. All are in product code DXQ (Blood Pressure Cuff). 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 Wuxi Medical Instrument Factory’s devices, and how often a recall has named them.
FDA decisions per year
1in 2011
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2011.
Planning a device like Wuxi Medical Instrument Factory’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 “Wuxi”
FDA records each applicant name separately; these may or may not be the same firm.