Industria Optica Rodenstock Chile S. A

FDA Device Registration & Listing · Santiago , Region Metropolitana, CL · Registration 3004848970

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
3004848970
FEI Number
3004848970
Entity Name
Industria Optica Rodenstock Chile S. A
City/State/Country
Santiago , Region Metropolitana, CL
Establishment Address
Avenida Beaucheff N 1581 Santiago, Santiago , Region Metropolitana 8370719, CL
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Rodenstock GmbHElsenheimer (Owner Number: 10061326)
Owner / Operator Contact Address
Elsenheimer Strasse 33, Munich, DE-BY 80687, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DNEye Scanner 3 (HKI) DNEye Scanner 2 DNEye Scanner 2+ VX120 VX118 Porche Design Sunglasses Rodenstock Sunglasses

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2024-08-21
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2024-08-21
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2021-03-17
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2021-04-27
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2019-10-08

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Rodenstock GmbHElsenheimer
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
K870750 Keeler Instruments, Inc. KEELER PULSAIR NON CONTACT TONOMETER 1987-03-17
K041546 Canon, Inc. DIGITAL FUNDUS CAMERA, MODEL CF-60DSI 2004-06-23
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004848970. Last updated year: 2026. Please use registration number 3004848970 when referencing this establishment in official correspondence.
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