CARL ZEISS MEDITEC INC

FDA Device Registration & Listing · DUBLIN, CA, US · Registration 2918630

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
2918630
FEI Number
2918630
Entity Name
CARL ZEISS MEDITEC INC
City/State/Country
DUBLIN, CA, US
Establishment Address
5300 Central Parkway, DUBLIN, CA 94568, US
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
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Humphrey Field Analyzer 3 (HFA3) Model: 830, 840, 850 860 CIRRUS Photo Models 600 and 800 Power Table Model AV 100 Power Table Model AV 220 Power Table Model HFA 230 Universal instrument table IT 760 Universal instrument table IT 760W.i Universal instrument table IT 1060.i Universal instrument table IT 1060 Universal instrument table IT 760.i Universal instrument table IT 760 W Power Table Model HFA 120 Power Table Model AV 120 Power Table Model HPT 120 Power Table Model CV-120 Power Table Model AV 240 Power Table Model CV-230 Power Table Model Stratus OCT CLARUS Model 500 Nerve Cirrus™ HD-OCT Model 6000 CLARUS (700) Nerve Fiber Analyzer Stratus OCT with RNFL Normative Database Humphrey Optical Coherence Tomography (OCT) Scanner VELARA Software CIRRUS HD-OCT Model 500 CIRRUS HD-OCT Model 5000 Cirrus HD OCT CLARUS Model 700 CIRRUS HD-OCT Model 400, 4000 CIRRUS HD-OCT Model 500, 5000

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2014-09-11
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2014-07-29
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2014-07-29
HRJ Table, Instrument, Powered, Ophthalmic Ophthalmic Class 1 886.4855 2013-01-21
QER Camera, Ophthalmic, Slit-Scanning Ophthalmic Class 2 886.1120 2019-02-05
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2009-09-02
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2009-09-02
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2024-05-31
QER Camera, Ophthalmic, Slit-Scanning Ophthalmic Class 2 886.1120 2025-05-09
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2009-07-15
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 1992-10-02
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 1992-10-02
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2008-04-10
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2008-04-10
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2021-01-04
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2015-12-07
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 1992-10-02
QER Camera, Ophthalmic, Slit-Scanning Ophthalmic Class 2 886.1120 2019-06-27
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2012-10-19
HJM Transilluminator, Ac-Powered Ophthalmic Class 2 886.1945 2017-11-17

Official Correspondent

Carl ZEISS Meditec AG (Jena)

US Agent Details

No US Agent registered (Local establishment).

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
9615010 CARL ZEISS MEDITEC AG (OBERKOCHEN) OBERKOCHEN Baden-Wurttemberg, DE
3004467263 FCI SUD MAPOU LECLEZIO GOODLANDS Riviere du Rempart, MU

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K882805 Coopervision-Cilco CILCO VILLASENOR PACHYMETER 1988-08-12
K791040 Shimadzu Corp. SECTOR SCANNER, SDU-100, COMPUTERIZED 1979-10-04
K162372 Qt Ultrasound, LLC QT Ultrasound Breast Scanner-1 2017-06-06

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
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.
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-0008-2018 Optovue, Inc. 2
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional, and 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 the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue with Normative Database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.
Z-0010-2018 Optovue, Inc. 2
iVue 500 with iScan, D216606. Product non-contact, high resolution tomographic imaging device. It is intended for in vivo imaging, axial cross-sectional and 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 500 with normative database is a quantitative tool for the comparison of retina, retinal nerve fiber layer, ganglion cell complex, and optic disc measurements to a database of known normal subjects. The iVue 500 with normative database is indicated for use as a device to aid in the diagnosis, documentation, and management of ocular health and diseases in the adult population.
Z-0003-2011 Verathon, Inc. 2
BVI 9600 Bladder Volume Instrument, Aorta Scan Mode The BladderScan BVI 9600 with AortaScan Mode is a user-selectable, dual-function ultrasound device that projects ultrasound energy either into the lower abdomen to obtain an image of the bladder for measuring bladder volume, or into the mid-abdomen to obtain an image of the abdominal aorta for aortic diameter measurements.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2918630. Last updated year: 2026. Please use registration number 2918630 when referencing this establishment in official correspondence.
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