Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010600252

FEI Number

3010600252

Entity Name

EXAMVISION A/S

City/State/Country

samsoe Midtjylland, DK

Establishment Address

Industrivej 11, samsoe Midtjylland 8305, DK

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ExamVision A/S (Owner Number: 10094210)

Owner / Operator Contact Address

Industrivej 11, samsø, DK-82 8305, DK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ExamVision Light System ExamVision Loupe System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2025-11-19
HJH	Loupe, Binocular, Low Power	Ophthalmic	Class 1	886.5120	2025-11-19

Official Correspondent

Renugadevi Mariappan

US Agent Details

Javier Odriozola Zalaf Business: SteamHealth Group Email: jodriozola@streamhealthgroup.com Phone: (833) 3824611

Related Public Records

Same Entity

ExamVision A/S

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010600252. Last updated year: 2026. Please use registration number 3010600252 when referencing this establishment in official correspondence.