FDA applicant
Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.
FDA records 1 decision for Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd. (Hangzhou, CN) in 2020: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). 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 Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2020
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
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