FDA applicant
T.K. Glove Products Co., Ltd.
FDA records 3 decisions for T.K. Glove Products Co., Ltd. (Thailand, TH) from 1989 to 1993: 3 510(k) clearances. All are in product code LYY (Latex Patient Examination Glove). No recall is linked to its devices.
FDA’s records also spell it “T.K. Glove Products”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided T.K. Glove Products Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for T.K. Glove Products Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like T.K. Glove Products 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