FDA applicant
Foshan Cicada Dental Instrument Co, Ltd.
FDA records 4 decisions for Foshan Cicada Dental Instrument Co, Ltd. (Foshan, CN) from 2019 to 2022: 4 510(k) clearances. Most are in product codes EBW (Controller, Foot, Handpiece And Cord) and EBZ (Activator, Ultraviolet, For Polymerization). Since 2016 its 510(k)s took a median of 523 days from receipt to decision, against 281 for FDA’s reviews in the same codes and years. 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 Foshan Cicada Dental Instrument Co, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2022
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2019.
Planning a device like Foshan Cicada Dental Instrument Co, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report