Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005895460

FEI Number

3005895460

Entity Name

SCHNUCHEL

City/State/Country

Holm Schleswig-Holstein, DE

Establishment Address

Bredhornweg 80, Holm Schleswig-Holstein 25488, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SCHNUCHEL (Owner Number: 10030756)

Owner / Operator Contact Address

Achter de Hoef 8, Hetlingen, DE-SH 25491, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Schnuchel

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2009-11-09

Official Correspondent

Wolf Schnuchel

US Agent Details

Alfonso Escobar Business: Page & Smith Opticians Email: myvisionps@msn.com Phone: (212) 7598560

Related Public Records

Same Entity

SCHNUCHEL

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 3005895460. Last updated year: 2026. Please use registration number 3005895460 when referencing this establishment in official correspondence.