Data / Medical devices / Ireland / Veryan Medical Limited

Veryan Medical Limited: FDA-registered device maker in Galway Galway(County), Ireland, 1 PMA approval

Veryan Medical Limited is registered with the FDA (registration 3011632150) in Galway Galway(County), Ireland. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated October 4, 2018. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3011632150

Address

Block 5, Parkmore East Business Park Galway Technology Park, Parkmore, Galway Galway(County), Ireland, H91 V0TX

Owner or operator

Veryan (10058865)

Roles

Manufacturer, Specification developer

First device listed

November 4, 2018

Registered through

2026

Brand names listed

BioMimics 3D Vascular Stent System

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 Stent, Superficial Femoral Artery

Updated February 19, 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.