Evoqua Water Technologies - South Windsor

FDA Device Registration & Listing · South Windsor, CT, US · Registration 3006029151

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
3006029151
FEI Number
3006029151
Entity Name
Evoqua Water Technologies - South Windsor
City/State/Country
South Windsor, CT, US
Establishment Address
88 Nutmeg Road, South Windsor, CT 06074, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Evoqua Water Technologies, LLC (Owner Number: 10057016)
Owner / Operator Contact Address
558 Clark Road, Tewksbury, MA 01876, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K994279
PMA Number
N/A

All Registered Proprietary Names

SDI Exchange Tanks

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 2018-02-09

Official Correspondent

Robert Dudek

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Evoqua Water Technologies, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3017974963 Evoqua Water Technologies - Milpitas Milpitas, CA, US
3004057358 Evoqua Water Technologies LLC Indianapolis, IN, US
3013507157 Evoqua Water Technologies - Jacksonville Jacksonville, FL, US
3019131 Evoqua Water Technologies LLC Minneapolis, MN, US

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006029151. Last updated year: 2026. Please use registration number 3006029151 when referencing this establishment in official correspondence.
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