FDA applicant

Danyang Chanxin Glasses Cases Factory

Danyang City, CN1 decision2016–20160 recalls

FDA records 1 decision for Danyang Chanxin Glasses Cases Factory (Danyang City, CN) in 2016: 1 510(k) clearance. All are in product code LRX (Case, Contact Lens). Its devices cite 1 predicate, 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, ophthalmic panel, where it files most

How often FDA has decided Danyang Chanxin Glasses Cases Factory’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Danyang Chanxin Glasses Cases Factory by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Danyang Chanxin Glasses Cases Factory’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 “Danyang”

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

Danyang Huayi Medical Supply & Equipment Co, Ltd. 3 Danyang Jumao Healthcare Equipment Co., Ltd. 2 Danyang Comed Healthcare Co., Ltd. 1 Danyang Sunco Machinery Co., Ltd. 1 Danyang Suntec Auto Parts Co., Ltd. 1

Danyang Chanxin Glasses Cases Factory

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Danyang”