FDA applicant
Implacil DE Bortoli Material Odontologico Ltda
FDA records 2 decisions for Implacil DE Bortoli Material Odontologico Ltda (Sao Paulo, BR) from 2020 to 2021: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 16 predicates, 1 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 Implacil DE Bortoli Material Odontologico Ltda’s devices, and how often a recall has named them.
FDA decisions per year
1in 2021
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Implacil DE Bortoli Material…’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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