Data / Medical devices / Brazil / Kenvue LTDA
Kenvue LTDA: FDA-registered device maker in Sao Jose dos Campos Sao Paulo, Brazil, 1 510(k) clearance
Kenvue LTDA is registered with the FDA (registration 3030196441) in Sao Jose dos Campos Sao Paulo, Brazil. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 22, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030196441
- Address
- Rodovia Presidente Dutra KM 154, Sao Jose dos Campos Sao Paulo, Brazil, 12240907
- Owner or operator
- KENVUE LTDA (8040525)
- Roles
- Manufacturer
- First device listed
- March 17, 2003
- Registered through
- 2026
- Brand names listed
- Band Aid, Reach
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Floss, Dental | JES | 1 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 22, 1995 | K954007 | PARALLEL | KGX | Substantially Equivalent | Johnson & Johnson Consumer Products, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 22, 1995. 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.