ActivePure Manufacturing LLC

FDA Device Registration & Listing · Bristol, VA, US · Registration 3003547411

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
3003547411
FEI Number
3003547411
Entity Name
ActivePure Manufacturing LLC
City/State/Country
Bristol, VA, US
Establishment Address
1300 Valley Dr, Bristol, VA 24201, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ActivePure Medical LLC (Owner Number: 10075792)
Owner / Operator Contact Address
14841 Dallas Parkway, Suite 500 - The Aberdeen Building, Dallas, TX 75254, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Aerus Medical Guardian ActivePure Medical Guardian

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRA Purifier, Air, Ultraviolet, Medical General Hospital Class 2 880.6500 2020-06-26

Official Correspondent

Andrew Eide

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ActivePure Medical 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 3003547411. Last updated year: 2026. Please use registration number 3003547411 when referencing this establishment in official correspondence.
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