Optomed

FDA Device Registration & Listing · Oulu Pohjois-Pohjanmaa, FI · Registration 3007710608

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
3007710608
FEI Number
3007710608
Entity Name
Optomed
City/State/Country
Oulu Pohjois-Pohjanmaa, FI
Establishment Address
Yrttipellontie 1, Oulu Pohjois-Pohjanmaa 90230, FI
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Optomed Oyj (Owner Number: 10029840)
Owner / Operator Contact Address
Yrttipellontie 1, Oulu, FI-14 90230, FI
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HAAG-STREIT FUNDUS MODULE 300 Bosch Eye cam posterior module Smartscope M5 EY3 Smartscope M5 ES1 Pictor Plus VISUSCOUT 100 Pictor Bosch Eye Camera Bosch Eye cam anterior module Bosch Eye Camera SWAN Optomed Aurora Camera with Aurora Retinal Module and Aurora Anterior Module Pictor Prestige Camera with Pictor Prestige Retina Module and Pictor Prestige Anterior Module Signal Camera Optomed Lumo Camera

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 2017-05-16
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2011-08-02
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2014-09-26
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2018-04-19
PJZ Camera, Ophthalmic, General-Use Ophthalmic Class 2 886.1120 2025-07-07

Official Correspondent

Jyri Leskela

US Agent Details

Theresa Matson Business: Optomed USA Inc. Email: theresa.matson@optomed.com Phone: (626) 4375950

Related Public Records

Same Entity

Optomed Oyj
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.

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3010000450 CRYSTALVUE MEDICAL CORPORATION Taoyuan Dist.,, TW
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007710608. Last updated year: 2026. Please use registration number 3007710608 when referencing this establishment in official correspondence.
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