510(k) Report

FDA applicant

Chongqing Rob Linka Science and Technology Co., Ltd.

Chongqing, CN4 decisions2023–20240 recalls

FDA records 4 decisions for Chongqing Rob Linka Science and Technology Co., Ltd. (Chongqing, CN) from 2023 to 2024: 4 510(k) clearances. Most are in product codes NUH (Stimulator, Nerve, Transcutaneous…) and NGX (Stimulator, Muscle, Powered, For Muscle…). Since 2016 its 510(k)s took a median of 154 days from receipt to decision, against 109 for FDA’s reviews in the same codes and years. 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, neurology panel, where it files most

How often FDA has decided Chongqing Rob Linka Science and Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

3in 2024

2023: 12024: 3
2023high 3 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Chongqing Rob Linka Science and Technology Co., Ltd. by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Chongqing”

FDA records each applicant name separately; these may or may not be the same firm.