HUMANITY LIFE EXTENSION, LLC

FDA Device Registration & Listing · Saint Paul, MN, US · Registration 3035108304

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
3035108304
FEI Number
3035108304
Entity Name
HUMANITY LIFE EXTENSION, LLC
City/State/Country
Saint Paul, MN, US
Establishment Address
545 Atwater Cir, Saint Paul, MN 55103, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Humanity Life Extension, LLC (Owner Number: 10092403)
Owner / Operator Contact Address
545 Atwater Circle, Saint Paul, MN 55103, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Humilty Precision Temperature Management System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWJ System, Thermal Regulating Cardiovascular Class 2 870.5900 2025-01-03

Official Correspondent

Shelly Amann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Humanity Life Extension, LLC
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
K171373 3M Company 3M Bair Hugger Model 675 Total Temperature Management System 2017-10-10
K083336 Smiths Medical Asd, Inc. LEVEL 1 SNUGGLE WARM ADULT UNDERBODY CONVECTIVE WARMING BLANKET, MODEL SW-2013, LEVEL 1 SNUGGLE WARM LEFT LATERAL 2009-06-03

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0035-2010 Cincinnati Sub-Zero Products Inc 2
WarmAir 135 Thermal Regulating System. Catalog Numbers: 86186-115 V, 06186-115 V (sold in the U.S.) and #86185-100 V ( not sold in the U.S.). Intended for warming patients before, during and after surgery, and other specialty procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035108304. Last updated year: 2026. Please use registration number 3035108304 when referencing this establishment in official correspondence.
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