PUREWAY COMPLIANCE, INC.

FDA Device Registration & Listing · Katy, TX, US · Registration 3011881552

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
3011881552
FEI Number
3011881552
Entity Name
PUREWAY COMPLIANCE, INC.
City/State/Country
Katy, TX, US
Establishment Address
2717 Commercial Center Blvd Ste 200, Katy, TX 77494, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
PureWay Compliance, Inc. (Owner Number: 10049948)
Owner / Operator Contact Address
2717 commercial center blvd cinco ranch, Katy, TX 77494, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K151249
PMA Number
N/A

All Registered Proprietary Names

PureWay Sharps Collector Container PureWay Sharps Collector Container

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMK Container, Sharps General Hospital Class 2 880.5570 2025-06-05
MMK Container, Sharps General Hospital Class 2 880.5570 2015-09-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PureWay Compliance, Inc.
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 3011881552. Last updated year: 2026. Please use registration number 3011881552 when referencing this establishment in official correspondence.
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