Data / Medical devices / Implant, Endosseous, Root-Form / Brazil
FDA-registered makers of Implant, Endosseous, Root-Form in Brazil: 5 establishments
5 establishments in Brazil are registered with the FDA to make Implant, Endosseous, Root-Form (product code DZE). 4 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Implant, Endosseous, Root-Form
- Product code
- DZE
- Country
- Brazil
Makers of Implant, Endosseous, Root-Form in Brazil
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| JJGC Industria e Comercio de Materiais Dentarios SA | Curitiba Parana, Brazil | Manufacturer | 24 | December 12, 2025 | 0 | 1 | 0 | api.fda.gov |
| S.I.N. Implant System Ltda | Sao Paulo, Brazil | Manufacturer | 15 | November 7, 2025 | 0 | 2 | 0 | api.fda.gov |
| Implacil De Bortoli Material Odontologico Ltda | Sao Paulo, Brazil | Manufacturer | 2 | May 26, 2021 | 0 | 0 | 0 | api.fda.gov |
| D.S.P. Industrial Eireli Epp | Campo Largo Parana, Brazil | Manufacturer | 1 | February 11, 2021 | 0 | 0 | 0 | api.fda.gov |
| Unidade De Esterilizacao Cotia Ltda. | Cotia Sao Paulo, Brazil | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.