FDA applicant
Shenzhen LE Medical Technology Co., Ltd.
FDA records 1 decision for Shenzhen LE Medical Technology Co., Ltd. (Shenzhen, CN) in 2024: 1 510(k) clearance. All are in product code DPS (Electrocardiograph). Its devices cite 1 predicate, 0 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 Shenzhen LE Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Shenzhen LE Medical 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