FDA applicant
Beijing Sano Laser S&T Development Co.,Ltd
FDA records 6 decisions for Beijing Sano Laser S&T Development Co.,Ltd (Beijing, CN) from 2020 to 2026: 6 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and NGX (Stimulator, Muscle, Powered, For Muscle…). Since 2016 its 510(k)s took a median of 122 days from receipt to decision, against 90 for FDA’s reviews in the same codes and years. Its devices cite 7 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 Beijing Sano Laser S&T Development 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 2020.
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