MED STORM INNOVATION AS

FDA Device Registration & Listing · Oslo, NO · Registration 3004545755

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004545755
FEI Number
3004545755
Entity Name
MED STORM INNOVATION AS
City/State/Country
Oslo, NO
Establishment Address
Gimle Terrasse 4, Oslo 0264, NO
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Med Storm Innovation AS (Owner Number: 10094333)
Owner / Operator Contact Address
Gimle Terrasse 4, Oslo, NO-03 0264, NO
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MedStorm Skin Conductance Response Measurement

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZO Device, Galvanic Skin Response Measurement Neurology Class 2 882.1540 2025-11-24

Official Correspondent

Turid Hoeysaeter

US Agent Details

Hanne Storm Email: hanne.storm@med-storm.com Phone: (617) 9132176

Related Public Records

Same Entity

Med Storm Innovation AS
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004545755. Last updated year: 2026. Please use registration number 3004545755 when referencing this establishment in official correspondence.
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