Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003184440

FEI Number

3003184440

Entity Name

Meiji Pharma Spain

City/State/Country

Alcala de Henares Madrid (Province), ES

Establishment Address

Avda. de Madrid 94, Alcala de Henares Madrid (Province) 28802, ES

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Meiji Pharma Spain S.A. (Owner Number: 10050736)

Owner / Operator Contact Address

Avda. de Madrid 94, Alcala de Henares, ES-M 28802, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P160057

All Registered Proprietary Names

GenVisc TriVisc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2015-12-21
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2018-10-03

Official Correspondent

No official correspondent registered.

US Agent Details

David Toledo-Velasquez Business: Channel-Markers Medical LLC Email: info@channel-markers.com Phone: (215) 9081357

Related Public Records

Same Entity

Meiji Pharma Spain S.A.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003184440. Last updated year: 2026. Please use registration number 3003184440 when referencing this establishment in official correspondence.