Rodenstock (Thailand) Co., Ltd.

FDA Device Registration & Listing · Ladkrabang Krung Thep Maha Nakhon, TH · Registration 3004443844

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
3004443844
FEI Number
3004443844
Entity Name
Rodenstock (Thailand) Co., Ltd.
City/State/Country
Ladkrabang Krung Thep Maha Nakhon, TH
Establishment Address
201-204 Chalongkrung, Ladkrabang Krung Thep Maha Nakhon 10520, TH
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Rodenstock GmbH (Owner Number: 10089627)
Owner / Operator Contact Address
Elsenheimer Strasse 33, Munich, DE-BY 80687, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

DNEye Scanner 2, DNEye Scanner 2+, VX118,VX120(HKX) DNEye Scanner 3 (HKI)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2023-12-22
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2025-01-20
HKX Tonometer, Ac-Powered Ophthalmic Class 2 886.1930 2024-08-20
HKI Camera, Ophthalmic, Ac-Powered Ophthalmic Class 2 886.1120 2024-08-20

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 GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3008396732 RODENSTOCK CR S.R.O. Plzensky Klatovy, CZ

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

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

Registration Number Establishment Name Location
3006755718 DONGGUAN YUEHENG OPTICAL CO. LTD. Dongguan Guangdong, CN
3015534032 BOLLE SAFETY INC Carlsbad, CA, US
3007675955 Carl Zeiss Vision Canada, Inc. Toronto Ontario, CA
1000428458 GKB OPHTHALMICS LIMITED - UNIT II North Goa Goa, IN
3038136215 MEIVISION (VIETNAM) CO., LTD Ho Chi Minh City, VN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004443844. Last updated year: 2026. Please use registration number 3004443844 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.