FDA applicant
Shenzhen Dongjilian Medical Tech Co., Ltd.
FDA records 2 decisions for Shenzhen Dongjilian Medical Tech Co., Ltd. (Shenzhen, CN) from 2022 to 2023: 2 510(k) clearances. All are in product code IRP (Massager, Powered Inflatable Tube). 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 Shenzhen Dongjilian Medical Tech Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2023
2022high 1 (2022) · low 0 (2024)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2022.
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