FDA applicant
Shenzhen Yimi Life-Technology Co., Ltd.
FDA records 2 decisions for Shenzhen Yimi Life-Technology Co., Ltd. (Shenzhen, CN) from 2019 to 2024: 2 510(k) clearances. All are in product code DQA (Oximeter). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Shenzhen Yimi Life Technology Co., Ltd.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Shenzhen Yimi Life-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 2019.
Planning a device like Shenzhen Yimi Life-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