Data / Medical devices / Wire, Orthodontic / Brazil
FDA-registered makers of Wire, Orthodontic in Brazil: 5 establishments
5 establishments in Brazil are registered with the FDA to make Wire, Orthodontic (product code DZC). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Wire, Orthodontic
- Product code
- DZC
- Country
- Brazil
Makers of Wire, Orthodontic in Brazil
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aditek Do Brasil, SA | CRAVINHOS Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dental Morelli Ltda. | SOROCABA Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthometric Ind. E Com. De Prod. Med. Odont. | Marilia Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tecnident Equipamentos Ortodonticos Ltda. | SAO CARLOS Sao Paulo, Brazil | Exporter to the US, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ultimate Do Brasil Importacao E Exportacao Ltda. | SAO JOSE DOS CAMPOS Sao Paulo, Brazil | Contract manufacturer | 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.