UREBLOCK

FDA Device Registration & Listing · Cienega de Flores Nuevo Leon, MX · Registration 3016510644

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016510644
FEI Number
3016510644
Entity Name
UREBLOCK
City/State/Country
Cienega de Flores Nuevo Leon, MX
Establishment Address
AVE DEL PARQUE NO. 2140 PARQUE INDUSTRIAL MONTERREY TECHNOLOGY PARK, Cienega de Flores Nuevo Leon 65550, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Ureblock S.A de C.V. (Owner Number: 10024159)
Owner / Operator Contact Address
Calle 4, No. 300 Fracc. Los Robles, URE780612C48, Zapopan, MX-JAL 45134, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Direct supply

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2008-01-08

Official Correspondent

No official correspondent registered.

US Agent Details

Liliana Gonzalez Business: Hessen Forwarding Email: liliana.gonzalez@hessen.com Phone: (956) 3122005

Related Public Records

Same Entity

Ureblock S.A de C.V.
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 3016510644. Last updated year: 2026. Please use registration number 3016510644 when referencing this establishment in official correspondence.
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