510(k) Report

FDA applicant

Suzhou Sen Sen Medical Supplies, Ltd.

Ontario, CA1 decision2003–20030 recalls

FDA records 1 decision for Suzhou Sen Sen Medical Supplies, Ltd. (Ontario, CA) in 2003: 1 510(k) clearance. All are in product code MQX (Needle, Acupuncture, Single Use). 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, general hospital panel, where it files most

How often FDA has decided Suzhou Sen Sen Medical Supplies, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Suzhou Sen Sen Medical Supplies, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Suzhou Sen Sen Medical Supplies, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Suzhou Sen Sen Medical Supplies, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • MQXNeedle, Acupuncture, Single Use1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K030190Carbo/Optimed Brand Acupuncture NeedlesSuzhou Sen Sen Medical Supplies, Ltd. · 2003

The one decision as Suzhou Sen Sen Medical Supplies, Ltd. →