KOWA CO. LTD. CHOFU

FDA Device Registration & Listing · Chofu Tokyo, JP · Registration 3011223751

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
3011223751
FEI Number
3011223751
Entity Name
KOWA CO. LTD. CHOFU
City/State/Country
Chofu Tokyo, JP
Establishment Address
3-1, Chofugaoka 3-chome, Chofu Tokyo 182-0021, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KOWA CO. LTD. (Owner Number: 8030217)
Owner / Operator Contact Address
4-14, Nihonbashi-honcho 3-chome, Chuo-ku, Tokyo, JP-13 1038433, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

KOWA VX-20 KOWA SL-17 KOWA VX-10a KOWA nonmyd WX KOWA SL-19 KOWA AP-7000 KOWA GENESIS-Df KOWA FM-600 KOWA APPLANATION TONOMETER HA-2 KOWA APPLANATION TONOMETER HA-1 KOWA VK-2s KOWA nonmyd 8 KOWA DR-1a

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 2012-02-23
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2012-02-23
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2014-04-10
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2009-07-06
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2011-04-12
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2022-12-01
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2003-12-24
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2009-08-10
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2009-08-10
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2007-11-05
NFJ System, Image Management, Ophthalmic Radiology Class 2 892.2050 2019-02-15
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2019-02-15
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2019-09-11
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2019-06-04

Official Correspondent

No official correspondent registered.

US Agent Details

Kraig McBride Business: Kowa Pharmaceuticals America, Inc. Email: fda@kowa.com Phone: (334) 2881288

Related Public Records

Same Entity

KOWA CO. LTD.
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
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23

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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011223751. Last updated year: 2026. Please use registration number 3011223751 when referencing this establishment in official correspondence.
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