FDA applicant

Maanshan Medical Instruments Co., Ltd.

Littleton, CO1 decision2005–20050 recalls

FDA records 1 decision for Maanshan Medical Instruments Co., Ltd. (Littleton, CO) in 2005: 1 510(k) clearance. All are in product code MQX (Needle, Acupuncture, Single Use). 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 Maanshan Medical Instruments Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maanshan Medical Instruments Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Maanshan Medical Instruments Co., 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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Other applicant names beginning “Maanshan”

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

Maanshan Bond Medical Instruments Co., Ltd. 1

Maanshan Medical Instruments Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Maanshan”