FDA applicant
Foshan Soco Precision Instrument Co., Ltd.
FDA records 1 decision for Foshan Soco Precision Instrument Co., Ltd. (Foshan, CN) in 2024: 1 510(k) clearance. All are in product code EFB (Handpiece, Air-Powered, Dental). 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 Foshan Soco Precision Instrument Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Foshan Soco Precision Instrument 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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