Optos Inc.

FDA Device Registration & Listing · Southborough, MA, US · Registration 3005744933

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
3005744933
FEI Number
3005744933
Entity Name
Optos Inc.
City/State/Country
Southborough, MA, US
Establishment Address
155 Northboro Rd Ste 12, Southborough, MA 01772, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OPTOS PLC (Owner Number: 9035556)
Owner / Operator Contact Address
QUEENSFERRY HOUSE, CARNEGIE, BUSINESS CAMPUS, DUNFERMLINE, FIFE, GB-NOTA KY11 8GR, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Monaco P200TE Panoramic P200T (Daytona) Daytona Panoramic 200T P200 200Dx PANORAMIC Optos SPECTRAL OCT/SLO P200TE 200Tx Panoramic 200MAAF

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2023-12-06
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2023-12-06
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2011-10-08
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2006-12-19
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2011-10-12
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2018-03-19
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2018-03-19
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2010-11-03

Official Correspondent

Alan Leitch

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OPTOS PLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
9617167 OPTOS PLC DUNFERMLINE, FIFE, GB

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04

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-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.

Similar Registrations

Registration Number Establishment Name Location
3008348697 Wild GmbH Voelkermarkt Karnten, AT
9617167 OPTOS PLC DUNFERMLINE, FIFE, GB
3009973692 Elemaster Spa lomagna Lecco, IT
3008422902 CENTERVUE Padova Veneto, IT
2918630 CARL ZEISS MEDITEC INC DUBLIN, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005744933. Last updated year: 2026. Please use registration number 3005744933 when referencing this establishment in official correspondence.
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