Data / Medical devices / Floss, Dental / Brazil
FDA-registered makers of Floss, Dental in Brazil: 5 establishments
5 establishments in Brazil are registered with the FDA to make Floss, Dental (product code JES). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Floss, Dental
- Product code
- JES
- Country
- Brazil
Makers of Floss, Dental in Brazil
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Colgate-Palmolive Industrial Ltda | Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Condor Nordeste In E Com Ltda - Filial Sul | Sao Bento do Sul Santa Catarina, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Condor S.A | Sao Bento do Sul Santa Catarina, Brazil | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kenvue LTDA | Sao Jose dos Campos Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rabbit Industria E Comercio De Produtos De Higiene Pessoal Ltda. | Londrina Parana, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.