FDA applicant
Luliang Hongruida Health Protection Technology Co., Ltd.
FDA records 2 decisions for Luliang Hongruida Health Protection Technology Co., Ltd. (Qujing, CN) from 2022 to 2024: 2 510(k) clearances. All are in product code LZA (Polymer Patient Examination Glove). Its devices cite 2 predicates, 1 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 Luliang Hongruida Health Protection Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2022.
Planning a device like Luliang Hongruida Health Protection…’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