510(k) Report

FDA applicant

Zhejiang Haisheng Medical Device Co., Ltd.

Shaoxing, CN2 decisions2015–20160 recalls

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, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

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

2015: 12016: 1
2015high 1 (2015) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Zhejiang Haisheng Medical Device Co., Ltd. by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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