Data / Medical devices / Brazil / Johnson & Johnson Do Brasil Industria E Comercio De Produtos Para Saude Ltda
Johnson & Johnson Do Brasil Industria E Comercio De Produtos Para Saude Ltda: FDA-registered device maker in Guarulhos Sao Paulo, Brazil, 2 510(k) clearances
Johnson & Johnson Do Brasil Industria E Comercio De Produtos Para Saude Ltda is registered with the FDA (registration 3013644499) in Guarulhos Sao Paulo, Brazil. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 18, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013644499
- Address
- Avenue Julia Gaiolli, Number 740 - T300 Hangar 7 e 8 - Agua Chata, Guarulhos Sao Paulo, Brazil, 07251-500
- Owner or operator
- ETHICON INC. (2210968)
- Roles
- Exporter to the US
- First device listed
- May 3, 2007
- Registered through
- 2026
- Brand names listed
- BONE WAX, Endoknot/Endoloop made with Coated Vicryl Endoknot/Endoloop made with PDS II Endoknot made with Ethibond Excel, VICRYL RAPIDE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Exporter to the US | accessdata.fda.gov |
| Suture, Absorbable, Synthetic, Polyglycolic Acid | GAM | 2 | Exporter to the US | accessdata.fda.gov |
| Wax, Bone | MTJ | U | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| December 18, 2003 | K033746 | MODIFIED COATED VICRYL* RAPIDE (POLYGLACTIN 910) SUTURE | GAM | Substantially Equivalent | ETHICON, Inc. | accessdata.fda.gov |
| October 31, 1984 | K843187 | CANNULA | GEA | Substantially Equivalent | ETHICON, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Surgical, General & Plastic Surgery
- All makers of Wax, Bone
- All makers of Suture, Absorbable, Synthetic, Polyglycolic Acid
Updated December 18, 2003. 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.