Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3024182169

FEI Number

3024182169

Entity Name

EYWA S.R.L.

City/State/Country

Rimini, IT

Establishment Address

Via Pietrarubbia 25/E, Rimini 47922, IT

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Eywa s.r.l. (Owner Number: 10094368)

Owner / Operator Contact Address

va Pietrarubhia 25/E, Rimimi, IT-RN 47922, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K243165

PMA Number

N/A

All Registered Proprietary Names

LIMFA Therapy System

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	2025-11-25

Official Correspondent

Thomas Lawson

US Agent Details

Thomas Lawson Email: drthomlawson@gmail.com Phone: (510) 2061794

Related Public Records

Same Entity

Eywa s.r.l.

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 3024182169. Last updated year: 2026. Please use registration number 3024182169 when referencing this establishment in official correspondence.