MW.FEP SPA

FDA Device Registration & Listing · San Giovanni in Persiceto Bologna, IT · Registration 3010394097

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
3010394097
FEI Number
3010394097
Entity Name
MW.FEP SPA
City/State/Country
San Giovanni in Persiceto Bologna, IT
Establishment Address
Via Modena 68, San Giovanni in Persiceto Bologna 40017, IT
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MW.FEP s.p.a. (Owner Number: 10044722)
Owner / Operator Contact Address
Via Modena 68, San Giovanni in Persiceto, IT-BO 40017, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CENTERVUE CENTERVUE CENTERVUE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HLI Ophthalmoscope, Ac-Powered Ophthalmic Class 2 886.1570 2014-05-26
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2014-05-26
MYC Ophthalmoscope, Laser, Scanning Ophthalmic Class 2 886.1570 2020-08-07
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2020-08-07
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2013-07-18

Official Correspondent

Lisa Giurissa

US Agent Details

STEVE WITTY Email: steve.witty@icare-world.com Phone: (844) 2134408

Related Public Records

Same Entity

MW.FEP s.p.a.
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
K142953 Optomedical Technologies GmbH OCT-Camera 2015-03-04
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
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-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 3010394097. Last updated year: 2026. Please use registration number 3010394097 when referencing this establishment in official correspondence.
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