Veolia Water Treatment & Solutions

FDA Device Registration & Listing · ARLINGTON, TX, US · Registration 3003550196

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
3003550196
FEI Number
3003550196
Entity Name
Veolia Water Treatment & Solutions
City/State/Country
ARLINGTON, TX, US
Establishment Address
1217 Corporate Dr W, ARLINGTON, TX 76006, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Veolia WTS Services, INC. (Owner Number: 10092834)
Owner / Operator Contact Address
1217 Corporate Drive W, Arlington, TX 76006, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FIP Subsystem, Water Purification Gastroenterology, Urology Class 2 876.5665 2026-03-20

Official Correspondent

David Chaudoin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Veolia WTS Services, INC.
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
K110578 Mar Cor Purification, Inc. MILLENIUM HX PORTABLE REVERSE OSMOSIS WATER PURIFICATION SYSTEM 2011-05-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0004-05 Ameriwater Inc 2
AmeriWater Portable RO+, model numbers MR01 and MR02. The device is a reverse osmosis system for dialysis.

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3015349756 DIALITY, INC. Irvine, CA, US
9611824 FRESENIUS MEDICAL CARE DEUTSCHLAND GMBH SCHWEINFURT Bavaria, DE
3010863450 AXIAL MEDICAL Ivyland, PA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003550196. Last updated year: 2026. Please use registration number 3003550196 when referencing this establishment in official correspondence.
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