FDA applicant
Sunpex Technology Co., Ltd.
FDA records 4 decisions for Sunpex Technology Co., Ltd. (Baltimore, MD) from 2002 to 2004: 4 510(k) clearances. Most are in product codes INI (Vehicle, Motorized 3-Wheeled) and ITI (Wheelchair, Powered). 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 Sunpex Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Sunpex Technology Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Sunpex Technology 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