C.S.O. S.R.L.

FDA Device Registration & Listing · Scandicci Firenze, IT · Registration 8020986

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
8020986
FEI Number
4196
Entity Name
C.S.O. S.R.L.
City/State/Country
Scandicci Firenze, IT
Establishment Address
VIA DEGLI STAGNACCI 12/E, Scandicci Firenze 50018, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
C.S.O. S.R.L. (Owner Number: 8020987)
Owner / Operator Contact Address
VIA DEGLI STAGNACCI 12/E, --, Scandicci, IT-NOTA 50018, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cobra Retina400 MS-39 C.S.O. CHAIR C.S.O. INSTRUMENT TABLE C.S.O. REFRACTING UNIT A900, F900 Surgical Microscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2014-07-09
MXK Device, Analysis, Anterior Segment Ophthalmic Class 2 886.1850 2023-09-27
OBO Tomography, Optical Coherence Ophthalmic Class 2 886.1570 2023-09-27
HME Chair, Ophthalmic, Ac-Powered Ophthalmic Class 1 886.1140 2000-02-04
HRJ Table, Instrument, Powered, Ophthalmic Ophthalmic Class 1 886.4855 1999-12-20
HMF Stand, Instrument, Ac-Powered, Ophthalmic Ophthalmic Class 1 886.1860 2000-02-04
HKY Tonometer, Manual Ophthalmic Class 2 886.1930 2008-12-03
HRM Microscope, Operating & Accessories, Ac-Powered, Ophthalmic General, Plastic Surgery Class 1 878.4700 2010-02-01

Official Correspondent

No official correspondent registered.

US Agent Details

David Biggins Business: Woodridge IBD LLC Email: david.w.biggins@gmail.com Phone: (716) 3167709

Related Public Records

Same Entity

C.S.O. S.R.L.
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.
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 8020986. Last updated year: 2026. Please use registration number 8020986 when referencing this establishment in official correspondence.
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