FDA applicant
Guangdong Jinme Medical Technology Co., Ltd.
FDA records 5 decisions for Guangdong Jinme Medical Technology Co., Ltd. (Foshan, CN) from 2017 to 2026: 5 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and DZI (Drill, Bone, Powered). Since 2016 its 510(k)s took a median of 287 days from receipt to decision, against 246 for FDA’s reviews in the same codes and years. Its devices cite 5 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Guangdong JINME Medical Technology Co., Ltd.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Guangdong Jinme Medical Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Guangdong Jinme Medical Technology…’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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