510(k) Report

FDA applicant

Vr Medical

Kunshan, CN2 decisions2011–20140 recalls

FDA records 2 decisions for Vr Medical (Kunshan, CN) from 2011 to 2014: 2 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and FPD (Tube, Feeding). Its devices cite 6 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, anesthesiology panel, where it files most

How often FDA has decided Vr Medical’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2011: 12014: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Vr Medical by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vr Medical’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?

  • CAHFilter, Bacterial, Breathing-Circuit1decision
  • FPDTube, Feeding1decision

Whose devices does it build on?

Its devices cite 6 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K132709VR Medical Heat and Moisture Exchanger and FilterVr Medical · 20141cites it

What has FDA decided for it lately?

  • K132709VR Medical Heat and Moisture Exchanger and FilterVr Medical · 2014
  • K110853VR Medical Enteral Oral SyringeVr Medical · 2011

All 2 as Vr Medical →