Kenvue LTDA

FDA Device Registration & Listing · Sao Jose dos Campos Sao Paulo, BR · Registration 3030196441

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3030196441
FEI Number
3030196441
Entity Name
Kenvue LTDA
City/State/Country
Sao Jose dos Campos Sao Paulo, BR
Establishment Address
Rodovia Presidente Dutra KM 154, Sao Jose dos Campos Sao Paulo 12240907, BR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KENVUE LTDA (Owner Number: 8040525)
Owner / Operator Contact Address
RODOVIA PRESIDENTE DUTRA, KM 154, SAO JOSE DOS CAMPOS, BR-SP 12240-907, BR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Band Aid Reach Band Aid

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2003-03-17
JES Floss, Dental Dental Class 1 872.6390 2004-01-14
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2011-12-28

Official Correspondent

Luiz Felipe Rodrigues

US Agent Details

Robert Mahler Email: RA-MCCUS-GROTMB@kenvue.com Phone: (848) 3546878

Related Public Records

Same Entity

KENVUE LTDA
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04
K882164 Arthur Blank & Co., Inc. FLOSS CARD 1988-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030196441. Last updated year: 2026. Please use registration number 3030196441 when referencing this establishment in official correspondence.
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