Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020775387

FEI Number

3020775387

Entity Name

OCCUTECH CO., LTD.

City/State/Country

Seongnam-si Gyeonggi, KR

Establishment Address

Star Tower #1308, 37, Sagimakgol-ro 62beon-gil, Jungwon-gu,, Seongnam-si Gyeonggi 13211, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

OccuTech Co., Ltd. (Owner Number: 10083039)

Owner / Operator Contact Address

Star Tower #1308, 37, Sagimakgol-ro 62beon-gil, Jungwon-gu,, Seongnam-si, KR-41 13211, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

OccuShields (Models: OccuShields T, OccuShields L, OccuShields M, OccuShields S)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2021-11-03

Official Correspondent

INCHANG SONG

US Agent Details

Jung Ryun Ahn Business: KMC USA, Inc Email: kmc.usa@kmcerti.com Phone: (646) 3576058

Related Public Records

Same Entity

OccuTech Co., Ltd.

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 3020775387. Last updated year: 2026. Please use registration number 3020775387 when referencing this establishment in official correspondence.