Data / Medical devices / Australia / Epiminder Limited

Epiminder Limited: FDA-registered device maker in Melbourne Victoria, Australia, 1 510(k) clearance

Epiminder Limited is registered with the FDA (registration 3039411139) in Melbourne Victoria, Australia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 17, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3039411139

Address

525 Collins Street, Suite 210, Melbourne Victoria, Australia, 3000

Owner or operator

Epiminder Limited (10093773)

Roles

Complaint file establishment, Specification developer

First device listed

July 8, 2025

Registered through

2026

Brand names listed

Minder

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

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Updated April 17, 2025. 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.