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Data / Medical devices / Spain / Meiji Pharma Spain

Meiji Pharma Spain: FDA-registered device maker in Alcala de Henares Madrid(Province), Spain, 2 PMA approvals

Meiji Pharma Spain is registered with the FDA (registration 3003184440) in Alcala de Henares Madrid(Province), Spain. It lists 1 device type. The FDA files 2 PMA approvals under its listings, the newest dated November 13, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003184440
Address
Avda. de Madrid 94, Alcala de Henares Madrid(Province), Spain, 28802
Owner or operator
Meiji Pharma Spain S.A. (10050736)
Roles
Complaint file establishment, Exporter to the US, Manufacturer
First device listed
December 21, 2015
Registered through
2026
Brand names listed
GenVisc, TriVisc

Devices it lists

DeviceProduct codeClassRoleSource
Acid, Hyaluronic, IntraarticularMOZ3Complaint file establishment, Exporter to the US, Manufactureraccessdata.fda.gov

PMA approvals

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

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
November 13, 2017P160057TRIVISCMOZ3May 20, 2025accessdata.fda.gov
September 2, 2015P140005GENVISC 850MOZ3May 20, 2025accessdata.fda.gov

Compare with other makers

Updated May 20, 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.