FDA applicant
Zhejiang Gongdong Medical Technology Co., Ltd.
FDA records 3 decisions for Zhejiang Gongdong Medical Technology Co., Ltd. (Taizhou, CN) from 2020 to 2025: 3 510(k) clearances. Most are in product codes MMK (Container, Sharps) and JSM (Culture Media, Non-Propagating Transport). Its devices cite 4 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 Zhejiang Gongdong Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Zhejiang Gongdong Medical Technology…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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