FDA applicant
Samsung Mobile Display Co., Ltd.
FDA records 5 decisions for Samsung Mobile Display Co., Ltd. (Houston, TX) from 2009 to 2011: 5 510(k) clearances. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/Digital…). Its devices cite 5 predicates, 2 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
How often FDA has decided Samsung Mobile Display Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
3in 2011
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2009.
Planning a device like Samsung Mobile Display 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 “Samsung”
FDA records each applicant name separately; these may or may not be the same firm.