FDA applicant
Huizhou Xiaoou Technology Co., Ltd.
FDA records 1 decision for Huizhou Xiaoou Technology Co., Ltd. (Huizhou, CN) in 2022: 1 510(k) clearance. All are in product code DQA (Oximeter). 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 Huizhou Xiaoou Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2022
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2022.
Planning a device like Huizhou Xiaoou 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) ReportOther applicant names beginning “Huizhou”
FDA records each applicant name separately; these may or may not be the same firm.