Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027645737

FEI Number

3027645737

Entity Name

YOU MAWO GMBH

City/State/Country

Konstanz Baden-Wurttemberg, DE

Establishment Address

Macairestrasse 3, Konstanz Baden-Wurttemberg 78467, DE

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

You Mawo GmbH (Owner Number: 10088459)

Owner / Operator Contact Address

Macairestrasse 3, Konstanz, DE-BW 78467, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

YOU MAWO brand; list of models attached; all models are available in plenty colours

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2023-07-26

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

You Mawo 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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3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027645737. Last updated year: 2026. Please use registration number 3027645737 when referencing this establishment in official correspondence.