Topcon Healthcare, Inc.

FDA Device Registration & Listing · Oakland, NJ, US · Registration 2242863

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
2242863
FEI Number
2242863
Entity Name
Topcon Healthcare, Inc.
City/State/Country
Oakland, NJ, US
Establishment Address
111 Bauer Dr, Oakland, NJ 07436, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Topcon Healthcare, Inc. (Owner Number: 2242863)
Owner / Operator Contact Address
111 Bauer Drive, Oakland, NJ 07436, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Harmony Synergy ODM AIT-250W; AIT-350W; AIT-650; IDS-300; AIT-W1; AIT-W2 CLOUD EZ Lite 2 OS-100; OS-200 OS-300; OS-400 IS-5000; CS-5; IS-5500 IS-6500 VisiChart II VisiChart OC-2200 OC-2300; OC-2400

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2018-10-10
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2016-12-16
HRJ Table, Instrument, Powered, Ophthalmic Ophthalmic Class 1 886.4855 1994-12-13
OUG Medical Device Data System General Hospital Class 1 880.6310 2014-10-27
HMD Chair, Ophthalmic, Manual Ophthalmic Class 1 886.1140 2008-01-14
HMF Stand, Instrument, Ac-Powered, Ophthalmic Ophthalmic Class 1 886.1860 1994-12-13
HOS Projector, Ophthalmic Ophthalmic Class 1 886.1680 2008-12-30
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2024-06-18
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2024-06-18
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2024-06-18
HME Chair, Ophthalmic, Ac-Powered Ophthalmic Class 1 886.1140 1994-12-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Topcon Healthcare, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3002808383 Topcon Yamagata Co., LTD West Factory Yamagata-ken, JP
9614661 TOPCON CORP. TOKYO, JP
3008729548 Topcon Yamagata Co., LTD Yamagata-KEN, JP

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
3011520729 INTELLIGENT RETINAL IMAGING SYSTEMS, INC. Pensacola, FL, US
9615030 Carl Zeiss Meditec AG (Jena) Jena Thuringia, DE
3008729548 Topcon Yamagata Co., LTD Yamagata-KEN, JP
1000181430 CANON INC. Kawasaki Kanagawa, JP
9617167 OPTOS PLC DUNFERMLINE, FIFE, GB
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2242863. Last updated year: 2026. Please use registration number 2242863 when referencing this establishment in official correspondence.
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