FDA applicant

Zhejiang Lingyang Medical Apparatus Co., Ltd.

Linhai, CN1 decision2022–20220 recalls

FDA records 1 decision for Zhejiang Lingyang Medical Apparatus Co., Ltd. (Linhai, CN) in 2022: 1 510(k) clearance. All are in product code MEG (Syringe, Antistick). 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, general hospital panel, where it files most

How often FDA has decided Zhejiang Lingyang Medical Apparatus Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Zhejiang Lingyang Medical Apparatus Co., Ltd. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Zhejiang Lingyang Medical Apparatus Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?