FDA applicant
Jiujiang Taixin Technology Co., Ltd.
FDA records 2 decisions for Jiujiang Taixin Technology Co., Ltd. (Ruichang City, CN) from 2021 to 2022: 2 510(k) clearances. Most are in product codes LZA (Polymer Patient Examination Glove) and FXX (Mask, Surgical). 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 Jiujiang Taixin Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2022
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like Jiujiang Taixin 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) Report