Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010363281

FEI Number

3010363281

Entity Name

EVERVIEW CORP

City/State/Country

Geumcheon-gu Seoul, KR

Establishment Address

(Gasan-dong), #1108, 254, Beotkkot-ro, Geumcheon-gu Seoul 08511, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

EVERVIEW CORP (Owner Number: 10048470)

Owner / Operator Contact Address

(Gasan-dong), #1108, 254, Beotkkot-ro, Geumcheon-gu, KR-11 08511, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Auto Chart Projector DCP-900 LCD VISUAL TEST CHART LUCID-LC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOS	Projector, Ophthalmic	Ophthalmic	Class 1	886.1680	2015-01-16
HOK	Screen, Tangent, Projection, Ac-Powered	Ophthalmic	Class 1	886.1810	2015-01-16

Official Correspondent

No official correspondent registered.

US Agent Details

Grace Kim Business: JS INTERNATIONAL HOLDING Email: ahn3060@naver.com Phone: (310) 5983012

Related Public Records

Same Entity

EVERVIEW CORP

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
9614661	TOPCON CORP.	TOKYO, JP
3009515444	GINO OPTICAL (SHANGHAI) CO., LTD.	Shanghai, CN
3033566	OCULUS, INC.	Arlington, WA, US
3015972897	INNOVA MEDICAL OPHTHALMICS	Toronto Ontario, CA
3004095901	LIANYUNGANG TIANNUO OPTICAL INSTRUMENT CO., LTD.	LIANYUNGANG Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010363281. Last updated year: 2026. Please use registration number 3010363281 when referencing this establishment in official correspondence.