RABBIT INDUSTRIA E COMERCIO DE PRODUTOS DE HIGIENE PESSOAL LTDA.

FDA Device Registration & Listing · Londrina Parana, BR · Registration 3006540944

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
3006540944
FEI Number
3006540944
Entity Name
RABBIT INDUSTRIA E COMERCIO DE PRODUTOS DE HIGIENE PESSOAL LTDA.
City/State/Country
Londrina Parana, BR
Establishment Address
Av. Dez de Dezembro, 6770 / Barracoes 01 a 12, Londrina Parana 86046-440, BR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Rabbit Industria e Comercio de Produtos de Higiene Pessoal L (Owner Number: 10089391)
Owner / Operator Contact Address
Av. Dez de Dezembro, 6770 / Barracoes 01 a 12, Londrina, BR-PR 86046-440, BR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Doctor Duck Children’s School Toothbrush Teen Booster Toothbrush Extreme Ice Toothbrush ADL Booster Toothbrush Romero Britto Toothbrush Doctor Duck Children’s Toothbrush Booster Dental Floss Children’s Booster Dental Floss Dental Floss Extreme Ice Dental Floss Doctor Duck Children’s Dental Floss Expanding Dental Floss Premium Dental Floss Romero Britto Dental Floss

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXZ Dental Hygiene Kit Dental Class 1 872.6855 2024-01-17
JES Floss, Dental Dental Class 1 872.6390 2023-12-04

Official Correspondent

Emerson Rolim de Jesus

US Agent Details

Lisa Capote Business: Capote Law Firm Email: lisa@capotelawfirm.com Phone: (786) 8715680

Related Public Records

Same Entity

Rabbit Industria e Comercio de Produtos de Higiene Pessoal L
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
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 3006540944. Last updated year: 2026. Please use registration number 3006540944 when referencing this establishment in official correspondence.
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