510(k) Report

FDA applicant

Vr Medical Technology Co., Ltd.

Zhouzhuang, CN2 decisions2016–20190 recalls

FDA records 2 decisions for Vr Medical Technology Co., Ltd. (Zhouzhuang, CN) from 2016 to 2019: 2 510(k) clearances. Most are in product codes FPD (Tube, Feeding) and PNR (Enteral Syringes With Enteral Specific…). Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Vr Medical Technology”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

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

FDA decisions per year

1in 2019

2016: 12019: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Vr Medical Technology Co., Ltd. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vr Medical Technology 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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