Data / Medical devices / Belgium / Nyxoah SA Milmort

Nyxoah SA Milmort: FDA-registered device maker in Herstal Liege, Belgium, 1 PMA approval

Nyxoah SA Milmort is registered with the FDA (registration 3030384719) in Herstal Liege, Belgium. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated August 8, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3030384719

Address

Val du Geer Facility Rue Haute Claire1, Herstal Liege, Belgium, 4041

Owner or operator

Nyxoah SA Mont Saint Guibert (10093936)

Roles

Manufacturer

First device listed

August 13, 2025

Registered through

2026

Brand names listed

Genio

Devices it lists

PMA approvals

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

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Updated July 30, 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.