FDA applicant

Jiangyin Caina Technology Co., Ltd.

Jiangyin, CN7 decisions2011–20170 recalls

FDA records 7 decisions for Jiangyin Caina Technology Co., Ltd. (Jiangyin, CN) from 2011 to 2017: 7 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FPA (Set, Administration, Intravascular). Its devices cite 7 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, general hospital panel, where it files most

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

FDA decisions per year

1in 2017

2011high 4 (2015) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Jiangyin Caina Technology Co., Ltd. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Jiangyin Caina 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.

See the 510(k) Report

Other applicant names beginning “Jiangyin”

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

Jiangyin East China Medical Technology Co., Ltd. 2 Jiangyin Jintech Biotech Co., Ltd. 1 Jiangyin Newrise Medical Equipment Co., Ltd. 1

Jiangyin Caina Technology Co., Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Jiangyin”