510(k) Report

FDA applicant

Qingdao Future Medical Technology Co., Ltd.

Qingdao, CN2 decisions2018–20250 recalls

FDA records 2 decisions for Qingdao Future Medical Technology Co., Ltd. (Qingdao, CN) from 2018 to 2025: 2 510(k) clearances. All are in product code CAF (Nebulizer (Direct Patient Interface)). Its devices cite 3 predicates, 1 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, anesthesiology panel, where it files most

How often FDA has decided Qingdao Future Medical Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2018: 12025: 1
2018high 1 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Qingdao Future Medical Technology Co., Ltd. by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • CAFNebulizer (Direct Patient Interface)2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 1 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.

  • K171549Intelligent Mesh NebulizerQingdao Future Medical Technology Co., Ltd. · 20183cite it

What has FDA decided for it lately?

  • K251659Mesh Nebulizer (H6)Qingdao Future Medical Technology Co., Ltd. · 2025
  • K171549Intelligent Mesh NebulizerQingdao Future Medical Technology Co., Ltd. · 2018

All 2 as Qingdao Future Medical Technology Co., Ltd. →