OPTOVUE, INC.

FDA Device Registration & Listing · San Jose, CA, US · Registration 3005950902

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
3005950902
FEI Number
3005950902
Entity Name
OPTOVUE, INC.
City/State/Country
San Jose, CA, US
Establishment Address
231 Charcot Avenue, San Jose, CA 95131, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
OPTOVUE, INC. (Owner Number: 9091799)
Owner / Operator Contact Address
231 Charcot Avenue, --, San Jose, CA 95131, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CA (Model: CAM) iVue 100 iVue RTVue XR OCT Avanti with AngioVue Software; or; AngioVue Imaging System AngioVue Imaging System RTVue Cam iVue NR iVue with NDB RTVue Model 100 and 200 iCam 100 iCam 12MP Avanti RTVue 100

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2013-02-22
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2010-04-29
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2016-03-04
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2016-03-04
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2013-02-21
MMQ Topographer, Corneal, Ac-Powered Ophthalmic Class 1 886.1350 2013-02-21
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2013-02-22
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2010-12-10
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2013-02-20
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2018-08-13
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2018-08-13
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2013-10-22

Official Correspondent

Peter Sparacio

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OPTOVUE, INC.
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
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
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-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-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-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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005950902. Last updated year: 2026. Please use registration number 3005950902 when referencing this establishment in official correspondence.
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