GREAT LIFE HEALTHCARE

FDA Device Registration & Listing · Arcadia, CA, US · Registration 3015209701

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
3015209701
FEI Number
3015209701
Entity Name
GREAT LIFE HEALTHCARE
City/State/Country
Arcadia, CA, US
Establishment Address
1108 S BALDWIN AVE STE 106, Arcadia, CA 91007, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Great Life Healthcare (Owner Number: 10059825)
Owner / Operator Contact Address
1108 S BALDWIN AVE STE 106, Arcadia, CA 91007, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Universal Therapy System(UTS) CONCI-AIRE 85 CONCI-AIRE 80 GlideXpert

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNM Mattress, Air Flotation, Alternating Pressure General Hospital Class 2 880.5550 2023-02-17
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2023-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Great Life Healthcare
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015209701. Last updated year: 2026. Please use registration number 3015209701 when referencing this establishment in official correspondence.
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