FDA applicant
Cheng Chang Development Co., Ltd.
FDA records 1 decision for Cheng Chang Development Co., Ltd. (Chang Hua Hsien, TW) in 1989: 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
How often FDA has decided Cheng Chang Development Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cheng Chang Development Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cheng Chang Development 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) ReportOther applicant names beginning “Cheng”
FDA records each applicant name separately; these may or may not be the same firm.