FDA applicant
Beijing L&Z Medical Technology Development Co., Ltd.
FDA records 3 decisions for Beijing L&Z Medical Technology Development Co., Ltd. (Beijing, CN) from 2023 to 2026: 3 510(k) clearances. Most are in product codes KPE (Container, I.V.) and PIF (Gastrointestinal Tubes With Enteral Specific…). 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 Beijing L&Z Medical Technology Development 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 2023.
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