Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017237915

FEI Number

3017237915

Entity Name

IRISBOND CROWDBONDING, S.L.

City/State/Country

Donostia San Sebastian Guipuzcoa, ES

Establishment Address

Avenida de Tolosa, 75, Planta 2, Donostia San Sebastian Guipuzcoa 20018, ES

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

IRISBOND CROWDBONDING, S.L. (Owner Number: 10093060)

Owner / Operator Contact Address

Avenida de Tolosa, 75, Planta 2, Donostia-San Sebastián, ES-SS 20018, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

OSKOL2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILQ	System, Communication, Powered	Physical Medicine	Class 2	890.3710	2025-03-25

Official Correspondent

Eduardo Jauregui

US Agent Details

VICTOR SANCHEZ ALTURA Business: PHARMA-BIO SERV, INC. Email: usagent@pbsvinc.com Phone: (787) 5072911

Related Public Records

Same Entity

IRISBOND CROWDBONDING, S.L.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0004-2016	Lifeline Systems, Incorporated	2	Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017237915. Last updated year: 2026. Please use registration number 3017237915 when referencing this establishment in official correspondence.