Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007275470

FEI Number

3007275470

Entity Name

JABBLA

City/State/Country

Gent Oost-Vlaanderen, BE

Establishment Address

Foreestelaan 3, Gent Oost-Vlaanderen 9000, BE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Jabbla (Owner Number: 10055228)

Owner / Operator Contact Address

Foreestelaan 3, Gent, BE-VOV 9000, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Eye Tracking Module TLS Tellus i6 Vibe Vibe 12 HeyPad Vibe 10 Tellus 6 Vibe 12+ Allora 3

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	2017-06-22

Official Correspondent

Jo Cremelie

US Agent Details

Kevin Shelton Business: Shelton Technologies and Resources, LLC Email: info@staraac.com Phone: (863) 6037827

Related Public Records

Same Entity

Jabbla

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 3007275470. Last updated year: 2026. Please use registration number 3007275470 when referencing this establishment in official correspondence.