FDA applicant
Smtp Technology Co., Ltd.
FDA records 3 decisions for Smtp Technology Co., Ltd. (Zhangjiagang, CN) in 2021: 3 510(k) clearances. Most are in product codes LFL (Instrument, Ultrasonic Surgical) and JDX (Instrument, Surgical, Sonic And…). Its devices cite 4 predicates, 1 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 Smtp Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
3in 2021
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like Smtp 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