Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008468035

FEI Number

3008468035

Entity Name

MICROCUBE, LLC

City/State/Country

Fremont, CA, US

Establishment Address

47853 Warm Springs Blvd, Fremont, CA 94539, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

MicroCube, LLC (Owner Number: 10033867)

Owner / Operator Contact Address

47853 Warm Springs Blvd, Fremont, CA 94539, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Minitouch 3.8 Era System Minitouch 3.8 Era Handpiece Minitouch Generator Minitouch

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MNB	Device, Thermal Ablation, Endometrial	Unknown	Class 3	N/A	2023-08-09
MNB	Device, Thermal Ablation, Endometrial	Unknown	Class 3	N/A	2010-10-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MicroCube, LLC

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 3008468035. Last updated year: 2026. Please use registration number 3008468035 when referencing this establishment in official correspondence.