Dr. Brown's Company

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3008138005

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
3008138005
FEI Number
3008138005
Entity Name
Dr. Brown's Company
City/State/Country
Saint Louis, MO, US
Establishment Address
4433 Fyler Ave., Saint Louis, MO 63116, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Dr. Brown's Company (Owner Number: 10033683)
Owner / Operator Contact Address
4433 Fyler Ave., Saint Louis, MO 63116, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Dr. Brown's Dr. Brown's Dr. Brown's Dr. Brown's Dr. Brown's powered toothbrush Dr. Brown's Dr. Brown’s natural flow double electric breast pump

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MEF Ring, Teething, Non-Fluid Filled Dental Class 1 872.5550 2014-12-22
HFS Shield, Nipple General Hospital Class 1 880.5630 2016-06-22
EFW Toothbrush, Manual Dental Class 1 872.6855 2014-12-22
FNN Nipple, Lambs Feeding General Hospital Class 1 880.5640 2015-06-29
JEQ Toothbrush, Powered Dental Class 1 872.6865 2025-03-26
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2025-12-19
HGX Pump, Breast, Powered Obstetrics/Gynecology Class 2 884.5160 2024-12-12

Official Correspondent

Li Wang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dr. Brown's Company
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3008819945 Dr. Brown's Company Bonne Terre, MO, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K190465 Hygeia II Medical Group, Inc. Evolve Breast Pump 2019-10-18
K021739 Limerick, Inc. LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 2003-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008138005. Last updated year: 2026. Please use registration number 3008138005 when referencing this establishment in official correspondence.
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