GOTTI SWITZERLAND GMBH

FDA Device Registration & Listing · Waedenswil Zurich, CH · Registration 3004097896

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
3004097896
FEI Number
3004097896
Entity Name
GOTTI SWITZERLAND GMBH
City/State/Country
Waedenswil Zurich, CH
Establishment Address
Steinacherstrasse 150, Waedenswil Zurich 8820, CH
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Gotti Switzerland GmbH (Owner Number: 10086138)
Owner / Operator Contact Address
Steinacherstrasse 150, Waedenswil, CH-ZH 8820, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Gotti Switzerland GOTTI GOTTI+NIEDERER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2022-10-18

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp. Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Gotti Switzerland GmbH
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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004097896. Last updated year: 2026. Please use registration number 3004097896 when referencing this establishment in official correspondence.
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