FDA applicant
Shenzhen Sanping Image Technology Co., Ltd.
FDA records 2 decisions for Shenzhen Sanping Image Technology Co., Ltd. (Shenzhen, CN) in 2025: 2 510(k) clearances. Most are in product codes EOQ (Bronchoscope (Flexible Or Rigid)) and FGB (Ureteroscope And Accessories, Flexible/Rigid). Its devices cite 3 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 Shenzhen Sanping Image Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2025.
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