Data / Medical devices / Cannula, Surgical, General & Plastic Surgery / Brazil
FDA-registered makers of Cannula, Surgical, General & Plastic Surgery in Brazil: 5 establishments
5 establishments in Brazil are registered with the FDA to make Cannula, Surgical, General & Plastic Surgery (product code GEA). 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
- Cannula, Surgical, General & Plastic Surgery
- Product code
- GEA
- Country
- Brazil
Makers of Cannula, Surgical, General & Plastic Surgery in Brazil
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Fabinject Industria E Comercio Importacao E Exportacao Ltda | Taubate Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Faga Medical Industria De Equipamentos E Instrumentos Medico Hospitalares Ltda Me | Bauru Sao Paulo, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ITM Industria de Tecnologias Medicas LTDA | CANOAS Rio Grande do Sul, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Johnson & Johnson do Brasil Ind. Com. de Prod. p/ Saude Ltda | SAO JOSE DOS CAMPOS Sao Paulo, Brazil | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schobell Industrial Ltda | Rio Claro Sao Paulo, Brazil | 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.