FDA applicant
China Xinxing Corp., Ltd.
FDA records 3 decisions for China Xinxing Corp., Ltd. (Beijing, CN) in 1989: 3 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). 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 China Xinxing Corp., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for China Xinxing Corp., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like China Xinxing Corp., 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) Report