Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008309602

FEI Number

3008309602

Entity Name

ESCHENBACH OPTIK GMBH + CO

City/State/Country

Nurnberg Bavaria, DE

Establishment Address

Fuerther Strasse 252, Nurnberg Bavaria D-90429, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Eschenbach Optik GmbH (Owner Number: 10031846)

Owner / Operator Contact Address

Fuerther Strasse 252, Nuernberg, DE-BY D-90429, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Eschenbach Optik, Magno Eschenbach Optik Eschenbach Optik, Magno Smartlux Eschenbach Optik

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HKK	Telescope, Spectacle, Low-Vision	Ophthalmic	Class 1	886.5870	2010-03-15
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2010-03-15
HJF	Magnifier, Hand-Held, Low-Vision	Ophthalmic	Class 1	886.5540	2010-03-15
HOT	Aid, Vision Image Intensification	Ophthalmic	Class 1	886.5910	2010-03-15

Official Correspondent

Matthias Anke

US Agent Details

Gina Carey Business: Eschenbach Optik of America, Inc Email: gcarey@eschenbach.com Phone: (203) 7021605

Related Public Records

Same Entity

Eschenbach Optik GmbH

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 3008309602. Last updated year: 2026. Please use registration number 3008309602 when referencing this establishment in official correspondence.