FDA applicant
Anhui Deepblue Medical Technology Co., Ltd.
FDA records 2 decisions for Anhui Deepblue Medical Technology Co., Ltd. (Hefei, CN) in 2024: 2 510(k) clearances. Most are in product codes MUI (Media, Coupling, Ultrasound) and LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). Its devices cite 2 predicates, 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 Anhui Deepblue Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Anhui Deepblue Medical Technology Co.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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