510(k) Report

FDA applicant

Wenzhou Longwan Medical Instrument Company

Flintville, TN1 decision2006–20060 recalls

FDA records 1 decision for Wenzhou Longwan Medical Instrument Company (Flintville, TN) in 2006: 1 510(k) clearance. All are in product code DXQ (Blood Pressure Cuff). 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 Wenzhou Longwan Medical Instrument Company’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wenzhou Longwan Medical Instrument Company since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wenzhou Longwan Medical Instrument Company by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DXQBlood Pressure Cuff1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K060871AS101, Blood Pressure CuffWenzhou Longwan Medical Instrument Company · 20061cites it

What has FDA decided for it lately?

  • K060871AS101, Blood Pressure CuffWenzhou Longwan Medical Instrument Company · 2006

The one decision as Wenzhou Longwan Medical Instrument Company →