PHELCOM TECHNOLOGIES

FDA Device Registration & Listing · Sao Carlos Sao Paulo, BR · Registration 3017175640

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
3017175640
FEI Number
3017175640
Entity Name
PHELCOM TECHNOLOGIES
City/State/Country
Sao Carlos Sao Paulo, BR
Establishment Address
Rua Jose Missali, 820, Santa Felicia, Sao Carlos Sao Paulo 13562-405, BR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Phelcom Technologies (Owner Number: 10072211)
Owner / Operator Contact Address
Rua Jose Missali, 820, Santa Felicia, Sao Carlos, BR-SP 13562-405, BR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Eyer 2 Essential Eyer Retinal Camera - M-STD Eyer 2 Basic EYER RETINAL CAMERA NM-STD Eyer 2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PJZ Camera, Ophthalmic, General-Use Ophthalmic Class 2 886.1120 2020-07-15
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2023-04-05
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2026-04-15

Official Correspondent

Flavio Vieira

US Agent Details

PASSARINI CRO AND REGULATORY SOLUTIONS LLC Email: usagent@passarini.com.br Phone: (786) 8496760

Related Public Records

Same Entity

Phelcom Technologies
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.

Similar Registrations

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3017758228 C-MER RAINSOPTICS LIMITED Hong Kong, HK
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017175640. Last updated year: 2026. Please use registration number 3017175640 when referencing this establishment in official correspondence.
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