Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043572677

FEI Number

3043572677

Entity Name

LYNK SOLUTEC INC.

City/State/Country

Seoul, KR

Establishment Address

150 Yeongdeungpo-ro, Yeongdeungpo-gu, Seoul, South Korea, 1203, Bldg. B, Seoul 07292, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Lynk Solutec Inc. (Owner Number: 10095083)

Owner / Operator Contact Address

150 Yeongdeungpo-ro, Yeongdeungpo-gu, Seoul, South Korea, 1203, Bldg. B, Seoul, KR-11 07292, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LYNKS Frontalis Sling

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HNM	Needle, Ophthalmic Suturing	Ophthalmic	Class 1	886.4350	2026-01-21

Official Correspondent

SoHyun Ahn

US Agent Details

David Hyun Jun Paek Email: dpaek.rennes@gmail.com Phone: (818) 9030660

Related Public Records

Same Entity

Lynk Solutec Inc.

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 3043572677. Last updated year: 2026. Please use registration number 3043572677 when referencing this establishment in official correspondence.