Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031563240

FEI Number

3031563240

Entity Name

GRASP AS

City/State/Country

OS Hordaland, NO

Establishment Address

Oyro 55, OS Hordaland 5200, NO

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

GRASP AS (Owner Number: 10091002)

Owner / Operator Contact Address

Bjellandsvegen 29, Sunde, NO-12 5450, NO

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Grasp Aware Grasp Device

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	2024-06-13

Official Correspondent

No official correspondent registered.

US Agent Details

Daniel Stoller Business: CENIT Consulting Email: dan.stoller@cenitconsulting.com Phone: (281) 3806919

Related Public Records

Same Entity

GRASP AS

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 3031563240. Last updated year: 2026. Please use registration number 3031563240 when referencing this establishment in official correspondence.