Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017084392

FEI Number

3017084392

Entity Name

LIVASSURED

City/State/Country

Leiden Zuid-Holland, NL

Establishment Address

Schipholweg 103, Leiden Zuid-Holland 2316 XC, NL

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Livassured (Owner Number: 10094699)

Owner / Operator Contact Address

Schipholweg 103, Leiden, NL-ZH 2316 XC, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K243199

PMA Number

N/A

All Registered Proprietary Names

NightWatch+ US

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
POS	Physiological Signal Based Seizure Monitoring System	Neurology	Class 2	882.1580	2025-12-17

Official Correspondent

Jolanda Oorthuizen

US Agent Details

Johannes Steensma Business: Taronga Technology Inc Email: johannes.steensma@tarongatech.com Phone: (321) 5432167

Related Public Records

Same Entity

Livassured

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3022175264	NEURO EVENT LABS OY	Tampere Pirkanmaa, FI
3012933969	EMPATICA S.r.l.	Milano, IT
3043349255	EpiWatch, Inc.	Baltimore, MD, US
3014886121	INTOPS CO.,LTD.	Suwon Gyeonggi, KR
3042639792	Unitron Medx LLC	Cary, NC, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017084392. Last updated year: 2026. Please use registration number 3017084392 when referencing this establishment in official correspondence.