510(k) Report

FDA applicant

Shenzhen Jumper Medical Equipment Co., Ltd.

Shenzhen, CN10 decisions2011–20230 recalls

FDA records 10 decisions for Shenzhen Jumper Medical Equipment Co., Ltd. (Shenzhen, CN) from 2011 to 2023: 10 510(k) clearances. Most are in product codes FLL (Continuous Measurement Thermometer) and DXN (System, Measurement, Blood-Pressure…). Since 2016 its 510(k)s took a median of 199 days from receipt to decision, against 199 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, cardiovascular panel, where it files most

How often FDA has decided Shenzhen Jumper Medical Equipment Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2011: 12013: 12014: 22017: 12018: 12019: 32023: 1
2011high 3 (2019) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Shenzhen Jumper Medical Equipment Co., Ltd. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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