FDA applicant
Zhejiang Richall Medical Technology Co., Ltd.
FDA records 2 decisions for Zhejiang Richall Medical Technology Co., Ltd. (Pujiang, CN) in 2024: 2 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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 Zhejiang Richall Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2024
2024high 2 (2024) · low 0 (2025)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
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