Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010045034

FEI Number

3010045034

Entity Name

SPUMATEX SL

City/State/Country

Crevillente Alicante, ES

Establishment Address

Ctra. Murcia - Alicante, 49,500km, Crevillente Alicante 03330, ES

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SPUMATEX SL (Owner Number: 10043583)

Owner / Operator Contact Address

Ctra. Murcia - Alicante, 49,500km, Crevillente, ES-A 03330, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2013-03-01

Official Correspondent

Victor Ferrandez

US Agent Details

Sam Shaffer Business: L&R USA INC. Email: sam.shaffer@us.LRmed.com Phone: (414) 8924157

Related Public Records

Same Entity

SPUMATEX SL

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 3010045034. Last updated year: 2026. Please use registration number 3010045034 when referencing this establishment in official correspondence.