FDA applicant
Dipped Products (Thailand), Ltd.
FDA records 3 decisions for Dipped Products (Thailand), Ltd. (Amphur Khun Nieng, TH) from 2005 to 2017: 3 510(k) clearances. Most are in product codes LZA (Polymer Patient Examination Glove) and LYY (Latex Patient Examination Glove). 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 “Dipped Products (Thailand) Limited”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Dipped Products (Thailand), Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Dipped Products (Thailand), 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) ReportOther applicant names beginning “Dipped”
FDA records each applicant name separately; these may or may not be the same firm.