Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010364377

FEI Number

3010364377

Entity Name

Flexor SA

City/State/Country

Barbera del Valles Barcelona, ES

Establishment Address

C/watt 3, 93 718 1612, Barbera del Valles Barcelona 08210, ES

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Flexor S.A. (Owner Number: 10043492)

Owner / Operator Contact Address

C/ watt 3, Barbera del Valles, ES-CT 08210, 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	2013-02-21

Official Correspondent

Antonia Busia

US Agent Details

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

Related Public Records

Same Entity

Flexor 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 3010364377. Last updated year: 2026. Please use registration number 3010364377 when referencing this establishment in official correspondence.