Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038620647

FEI Number

3038620647

Entity Name

KISO EHF

City/State/Country

Reykjavik, IS

Establishment Address

Hatun 12, Reykjavik 105, IS

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Kiso ehf (Owner Number: 10093544)

Owner / Operator Contact Address

Hatun 12, Reykjavík, IS-55 105, IS

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KineMotion

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2025-06-02

Official Correspondent

Baldur Thorgilsson

US Agent Details

Rives Bird Business: Kiso INC Email: rives@rivesconsult.com Phone: (319) 2143032

Related Public Records

Same Entity

Kiso ehf

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
K873418	Bodylog, Inc.	BODYLOG STRESS REDUCTION PACKAGE	1987-12-17
K792659	Bio-Feedback Systems, Inc.	FEEDBACK EDR SYSTEM MODEL ME-1	1980-01-09

Similar Registrations

Registration Number	Establishment Name	Location
3013263129	2BREATHE TECHNOLOGIES LTD	Raanana Central, IL
3012164803	NFANT LABS Inc	Port Richey, FL, US
3011255064	RAYONEX BIOMEDICAL GMBH	Lennestadt North Rhine-Westphalia, DE
3005196642	HARMONIC ENERGETIC TECHNOLOGIES, LLC	Liverpool, NY, US
3004642067	NEUROCONN GMBH	Ilmenau Thuringia, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038620647. Last updated year: 2026. Please use registration number 3038620647 when referencing this establishment in official correspondence.