FDA applicant
Riton 3D Technology Co., Ltd.
FDA records 1 decision for Riton 3D Technology Co., Ltd. (Guangzhou, CN) in 2024: 1 510(k) clearance. All are in product code EBI (Resin, Denture, Relining, Repairing, Rebasing). 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 Riton 3D Technology 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 Riton 3D Technology 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