Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010400793

FEI Number

3008382474

Entity Name

Laboratoires Chemineau

City/State/Country

VOUVRAY Indre-et-Loire, FR

Establishment Address

93 route de Monnaie, VOUVRAY Indre-et-Loire 37210, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Laboratoires Chemineau (Owner Number: 10044335)

Owner / Operator Contact Address

93 route de Monnaie, Vouvray, FR-37 37210, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Afrin® Saline Burst Extra Strength Daily Nasal Mist Afrin® Saline Burst Moisturizing Daily Nasal Mist Childrens Afrin® Saline Moisturizing Daily Nasal Mist Aquoral

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2025-02-21
LFD	Saliva, Artificial	Unknown	Class U	N/A	2013-05-28

Official Correspondent

Axelle Prieur-Blanc

US Agent Details

Victoria Pankovich Business: EAS Consulting Group, LLC Email: usagent@easconsultinggroup.com Phone: (571) 4475500

Related Public Records

Same Entity

Laboratoires Chemineau

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010400793. Last updated year: 2026. Please use registration number 3010400793 when referencing this establishment in official correspondence.