510(k) Report

FDA applicant

Jiangsu Vedkang Medical Science and Technology Co., Ltd.

Changzhou, CN7 decisions2022–20240 recalls

FDA records 7 decisions for Jiangsu Vedkang Medical Science and Technology Co., Ltd. (Changzhou, CN) from 2022 to 2024: 7 510(k) clearances. Most are in product codes PKL (Hemostatic Metal Clip For The Gi Tract) and KNS (Unit, Electrosurgical, Endoscopic (With Or…). Since 2016 its 510(k)s took a median of 214 days from receipt to decision, against 206 for FDA’s reviews in the same codes and years. Its devices cite 6 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, gastroenterology and urology panel, where it files most

How often FDA has decided Jiangsu Vedkang Medical Science and Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

3in 2024

2022: 22023: 22024: 3
2022high 3 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Jiangsu Vedkang Medical Science and Technology Co., Ltd. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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