FDA applicant
Medimecca Co., Ltd.
FDA records 4 decisions for Medimecca Co., Ltd. (Seoul, KR) from 2013 to 2020: 4 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 5 predicates, 2 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 Medimecca Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2020
2013high 2 (2013) · low 0 (2014)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2013.
Planning a device like Medimecca 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