CARL ZEISS MEDITEC AG (Munich)

FDA Device Registration & Listing · Muenchen Bavaria, DE · Registration 3009746052

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
3009746052
FEI Number
3009746052
Entity Name
CARL ZEISS MEDITEC AG (Munich)
City/State/Country
Muenchen Bavaria, DE
Establishment Address
Kistlerhof Strasse 75, Muenchen Bavaria 81379, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Carl Zeiss Meditec AG (Jena) (Owner Number: 9053564)
Owner / Operator Contact Address
Goeschwitzer Strasse 51-52, Jena, DE-TH 07745, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Retina Workplace Retina Workplace 2 CALLISTO eye Panel PC FORUM Archive and Viewer FORUM Assist match FORUM Archive IOLMASTER 500 with Option Reference Image IOLMASTER 500 with Reference Image mode Zeiss Cataract Suite Markerless FORUM FORUM Viewer App

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2019-07-29
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2019-07-29
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2019-07-29
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2017-06-28
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2017-06-28
LMD System, Digital Image Communications, Radiological Radiology Class 1 892.2020 2003-12-29
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2009-04-23
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic General, Plastic Surgery Class 1 878.4700 2016-03-08
EPT Microscope, Surgical General, Plastic Surgery Class 1 878.4700 2016-03-08
HMR Marker, Ocular Ophthalmic Class 1 886.4570 2016-03-08
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2016-03-08
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2016-03-08
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2022-08-15
NFG Device, Communications, Images, Ophthalmic Radiology Class 1 892.2020 2003-12-29

Official Correspondent

Carl ZEISS Meditec AG (Jena)

US Agent Details

Paul Swift Business: CARL ZEISS MEDITEC USA, INC. Email: fdaagent.med.us@zeiss.com Phone: (817) 9258507

Related Public Records

Same Entity

Carl Zeiss Meditec AG (Jena)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3015534077 Carl Zeiss Meditec Digital Innovations Inc Temple, TX, US
3032734659 Carl Zeiss Meditec (Suzhou) Co., Ltd. Suzhou Jiangsu, CN
3010126268 Carl Zeiss Meditec Production, LLC. Ontario, CA, US
2918630 CARL ZEISS MEDITEC INC DUBLIN, CA, US
9615010 CARL ZEISS MEDITEC AG (OBERKOCHEN) OBERKOCHEN Baden-Wurttemberg, DE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0024-2013 Optovue Inc. 2
Reference materials "RETINAL OCT Analysis and Interpretation Method" shipped with iVue System (K091404) and the "Retina Poster" shipped with iVue System (K091404) and RTVue Systems (K101505); Models: iVue-100, RTVue-100; The physical Product is manufactured and distributed by Optovue, Inc. Fremont, CA The product is an optical coherence tomography system indicated for the in vivo imaging and measurement of the retina, retinal nerve fiber layer, optic disk, and for cornea and anterior eye scans as an aid in the diagnosis and management of retinal disease.
Z-0009-2018 Optovue, Inc. 2
iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolution digital imaging device which is suitable for photographing, displaying and storing images of the retina and external areas of the eye to be evaluated under non-mydriatic conditions. The iCam takes digital images of the posterior and external structures of the eye without the use of a mydriatic agent and is intended for use as an aid to clinicians in the evaluation, diagnosis and documentation of ocular health. iCam provides images only and does not provide any diagnostic, pathological analysis or classification of ocular health or disease. AND iVue with Normative Database (K121739) - The iVue is a noncontact, high resolution optical coherence tomography system intended for in vivo imaging, axial cross-sectional, three-dimensional imaging and measurement of anterior and posterior. ocular structures, including retina, retinal nerve fiber layer, ganglion cell complex (GCC), optic disc, cornea, and anterior chamber of the eye. The iVue with Normative Database is a quantitative tool for comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects.

Similar Registrations

Registration Number Establishment Name Location
3008729548 Topcon Yamagata Co., LTD Yamagata-KEN, JP
3010000450 CRYSTALVUE MEDICAL CORPORATION Taoyuan Dist.,, TW
9614661 TOPCON CORP. TOKYO, JP
3008348697 Wild GmbH Voelkermarkt Karnten, AT
3006809695 Leica Microsystems NC, Inc. Durham, NC, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009746052. Last updated year: 2026. Please use registration number 3009746052 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.