Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029904430

FEI Number

3029904430

Entity Name

MAGNES AG

City/State/Country

Zurich, CH

Establishment Address

Hardturmstrasse 253, Zurich 8005, CH

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Magnes AG (Owner Number: 10089002)

Owner / Operator Contact Address

2261 Market St, STE 5508, San Francisco, CA 94114, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Nushu

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JFC	System, Pressure Measurement, Intermittent	Physical Medicine	Class 1	890.1600	2023-11-01

Official Correspondent

Olgac Ergeneman

US Agent Details

Veronica Besmer Email: veronica@besmer.com Phone: (415) 4411775

Related Public Records

Same Entity

Magnes AG

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 3029904430. Last updated year: 2026. Please use registration number 3029904430 when referencing this establishment in official correspondence.