PUREFLOW, LLC

FDA Device Registration & Listing · Salt Lake City, UT, US · Registration 3042365416

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
3042365416
FEI Number
3042365416
Entity Name
PUREFLOW, LLC
City/State/Country
Salt Lake City, UT, US
Establishment Address
726 W 500 N, Salt Lake City, UT 84116, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PureFlow, LLC (Owner Number: 10094194)
Owner / Operator Contact Address
726 W 500 N, Salt Lake City, UT 84116, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PureFlow Evacuation Valve

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNX Device, Incontinence, Urosheath Type, Non-Sterile Gastroenterology, Urology Class 1 876.5250 2025-11-18

Official Correspondent

David Rawlins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PureFlow, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042365416. Last updated year: 2026. Please use registration number 3042365416 when referencing this establishment in official correspondence.
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