FDA applicant
Shangdong Zibo Shanchuan Medical Instruments Co.
FDA records 2 decisions for Shangdong Zibo Shanchuan Medical Instruments Co. (Houston, TX) from 2003 to 2009: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and LYZ (Vinyl Patient Examination Glove). Its devices cite 2 predicates, 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 Shangdong Zibo Shanchuan Medical Instruments Co.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2009
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Shangdong Zibo Shanchuan Medical…’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 “Shangdong”
FDA records each applicant name separately; these may or may not be the same firm.