510(k) Report

FDA applicant

Implacil DE Bortoli Material Odontologico Ltda

Sao Paulo, BR2 decisions2020–20210 recalls

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, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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

2020: 12021: 1
2020high 1 (2020) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Implacil DE Bortoli Material Odontologico Ltda by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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