FDA applicant

Kaen Yang Industry Co., Ltd.

Bangkok 10900 Thailand, TH1 decision1990–19900 recalls

FDA records 1 decision for Kaen Yang Industry Co., Ltd. (Bangkok 10900 Thailand, TH) in 1990: 1 510(k) clearance. All are in product code LYY (Latex Patient Examination Glove). 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 Kaen Yang Industry Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kaen Yang Industry Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kaen Yang Industry Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kaen Yang Industry 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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Other applicant names beginning “Kaen”

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

Kaen Yih Enterprise Co., Ltd. 1

Kaen Yang Industry Co., Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kaen”