CARECUBES, INC.

FDA Device Registration & Listing · Arden Hills, MN, US · Registration 3038166862

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
3038166862
FEI Number
3038166862
Entity Name
CARECUBES, INC.
City/State/Country
Arden Hills, MN, US
Establishment Address
4440 Round Lake Rd W, Arden Hills, MN 55112, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Carecubes, Inc. (Owner Number: 10092995)
Owner / Operator Contact Address
4440 Round Lake Rd W, Arden Hills, MN 55112, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Carecube Negative Pressure Isolation Chamber

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LGM Chamber, Patient Isolation General Hospital Class 2 880.5450 2025-03-14

Official Correspondent

Becky Anderson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Carecubes, Inc.
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 3038166862. Last updated year: 2026. Please use registration number 3038166862 when referencing this establishment in official correspondence.
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