Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023205383

FEI Number

3023205383

Entity Name

I-MOTION GROUP GLOBAL IBERICA SL.

City/State/Country

Madrid, ES

Establishment Address

Calle Labradores 13, Boadilla del Monte, Madrid 28660, ES

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

I-MOTION GROUP GLOBAL IBERICA SL. (Owner Number: 10085323)

Owner / Operator Contact Address

Calle Labradores 13, Boadilla del Monte, Madrid, ES-MD 28660, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K212413

PMA Number

N/A

All Registered Proprietary Names

I-Shape Esthetic I-MOTION I-Model I-Shape Sport I-HomeFit SQAI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2022-06-03

Official Correspondent

Jose Luis Soto Belloso

US Agent Details

Victoria Pankovich Business: EAS Consulting Group, LLC Email: usagent@easconsultinggroup.com Phone: (571) 4475500

Related Public Records

Same Entity

I-MOTION GROUP GLOBAL IBERICA SL.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023205383. Last updated year: 2026. Please use registration number 3023205383 when referencing this establishment in official correspondence.