FDA applicant
Beijing Sincoheren Science and Technology Development Co.
FDA records 2 decisions for Beijing Sincoheren Science and Technology Development Co. (Beijing, CN) in 2017: 2 510(k) clearances. Most are in product codes ONG (Powered Laser Surgical Instrument With…) and GEX (Powered Laser Surgical Instrument). 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 Beijing Sincoheren Science and Technology Development Co.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
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