KEELER LTD.

FDA Device Registration & Listing · WINDSOR, BERKSHIRE Windsor and Maidenhead, GB · Registration 1000391004

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
1000391004
FEI Number
1000391004
Entity Name
KEELER LTD.
City/State/Country
WINDSOR, BERKSHIRE Windsor and Maidenhead, GB
Establishment Address
CLEWER HILL RD., WINDSOR, BERKSHIRE Windsor and Maidenhead SL4 4AA, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KEELER LTD. (Owner Number: 9011500)
Owner / Operator Contact Address
CLEWER HILL RD., WINDSOR, BERKSHIRE, GB-NOTA SL4 4AA, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2018-12-11
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2010-02-06
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2015-12-01
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2011-02-02
MMQ Topographer, Corneal, Ac-Powered Ophthalmic Class 1 886.1350 2022-03-08
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2013-07-05
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2020-05-01
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2008-03-26
HOQ Grid, Amsler Ophthalmic Class 1 886.1330 2008-03-26
HJM Transilluminator, Ac-Powered Ophthalmic Class 2 886.1945 2008-03-26
HRN Unit, Cryophthalmic, Ac-Powered Ophthalmic Class 2 886.4170 2008-03-26
HIT Tester, Color Vision Ophthalmic Class 1 886.1170 2008-03-26
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2008-03-26
HQF Laser, Ophthalmic Ophthalmic Class 2 886.4390 2025-03-26
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2008-03-26
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2019-03-12
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2007-12-11
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2007-12-11
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2021-07-01
HQF Laser, Ophthalmic Ophthalmic Class 2 886.4390 2021-07-01
HJO Biomicroscope, Slit-Lamp, Ac-Powered Ophthalmic Class 2 886.1850 2012-12-11
HRN Unit, Cryophthalmic, Ac-Powered Ophthalmic Class 2 886.4170 2014-01-03
EBA Light, Surgical Headlight Dental Class 1 872.4630 2005-11-09
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2024-09-04
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2008-03-26
ITX Transducer, Ultrasonic, Diagnostic Radiology Class 2 892.1570 2025-09-19
IYO System, Imaging, Pulsed Echo, Ultrasonic Radiology Class 2 892.1560 2025-09-19
HKL Retinoscope, Ac-Powered Ophthalmic Class 2 886.1780 2008-03-26
HJH Loupe, Binocular, Low Power Ophthalmic Class 1 886.5120 2008-03-26
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2008-03-26
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2014-09-18
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2008-12-16

Official Correspondent

Claudia Hill

US Agent Details

Claudia Hill Business: Keeler USA Email: chill@keelerusa.com Phone: (610) 8890200

Related Public Records

Same Entity

KEELER 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
K870750 Keeler Instruments, Inc. KEELER PULSAIR NON CONTACT TONOMETER 1987-03-17
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K834060 F. & F. Koenigkramer RELIANCE OPHTHALMIC SLIT LAMP R-083 1984-02-04
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30

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-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-0005-2014 PhotoMedex, Inc. 2
The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018 Medtronic Navigation, Inc. 2
VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000391004. Last updated year: 2026. Please use registration number 1000391004 when referencing this establishment in official correspondence.
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