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Sign in to claim this brandLABORATOIRES QUINTON INTERNATIONAL SL
US
Last updated May 31, 2026
What LABORATOIRES QUINTON INTERNATIONAL SL makes
The company produces sterile nasal irrigation saline solutions designed for daily nasal hygiene, including formulations for pediatric use and enhanced action. These products are packaged in 100 ml single-use containers and are intended for nasal cleansing and moisture maintenance.
The portfolio consists of Class I medical devices, which are subject to FDA regulation under the Unique Device Identifier (UDI) system. These products are listed in the FDA’s UDI database and comply with applicable U.S. regulatory requirements for over-the-counter nasal irrigation solutions.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Laboratoires Quinton International SL manufacture?
Laboratoires Quinton International SL specializes in sterile nasal irrigation saline solutions. These products are formulated for daily nasal hygiene, including specific variants like pediatric and enhanced-action versions. The devices are packaged in single-use 100 ml containers and are designed to cleanse and maintain nasal moisture.
Where is Laboratoires Quinton International SL based?
The company, Laboratoires Quinton International SL, is based in the United States. This location influences its regulatory compliance, particularly with U.S. medical device requirements.
Which regulatory registries list the devices manufactured by Laboratoires Quinton International SL?
The devices produced by Laboratoires Quinton International SL are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices under FDA oversight, ensuring traceability and compliance with U.S. regulatory standards.
How are the devices made by Laboratoires Quinton International SL classified under U.S. regulations?
The devices manufactured by Laboratoires Quinton International SL fall under Class I classification in the U.S. regulatory system. Class I devices are generally considered low-risk and are subject to general controls, including good manufacturing practices and labeling requirements. This classification aligns with their use as over-the-counter nasal irrigation solutions.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 563461441
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Eau de Quinton Pediatric Nasal Hygiene 100 ml | PT371 | FDA UDI | Class I | Active |
| Eau de Quinton Action Plus Nasal Hygiene 100 ml | PT373 | FDA UDI | Class I | Active |
| Eau de Quinton Daily Nasal Hygiene 100 ml | PT372 | FDA UDI | Class I | Active |
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