FDA applicant
Zhejiang Haisheng Medical Device Co., Ltd.
FDA records 2 decisions for Zhejiang Haisheng Medical Device Co., Ltd. (Shaoxing, CN) from 2015 to 2016: 2 510(k) clearances. Most are in product codes DRS (Transducer, Blood-Pressure, Extravascular) and CAH (Filter, Bacterial, Breathing-Circuit). 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 Zhejiang Haisheng Medical Device Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2016
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2015.
Planning a device like Zhejiang Haisheng Medical Device Co.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report