Data / Medical devices / United States / Microcube, LLC

Microcube, LLC: FDA-registered device maker in Fremont, CA, United States, 1 PMA approval

Microcube, LLC is registered with the FDA (registration 3008468035) in Fremont, CA, United States. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated July 28, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3008468035

Address

47853 Warm Springs Blvd, Fremont, CA, United States, 94539

Owner or operator

MicroCube, LLC (10033867)

Roles

Manufacturer, Manufacturer for export

First device listed

October 12, 2010

Registered through

2026

Brand names listed

Minitouch, Minitouch 3.8 Era Handpiece, Minitouch 3.8 Era System, Minitouch Generator

Devices it lists

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Compare with other makers

• All makers of Device, Thermal Ablation, Endometrial

Updated July 13, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.