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OFFICIAL OPENFDA FEI RECORDFEI: 3013501671Reg Yr: 2027South Korea (KR)

LG ELECTRONICS INC.

Official US Food and Drug Administration (FDA) Establishment Registration & Device/Facility Listing dossier for LG ELECTRONICS INC. (FEI 3013501671). Use this record to cross-check CBP ACE Affirmation of Compliance codes (`DEV` / `DFE` / `FEI`), verify the designated US Agent on file, and subscribe to automated Import Alert (DWPE) monitoring.

Registered Facility Address

168, Suchul-daero, Gyeongsangbuk-do

Gumi-si Gyeongbuk, South Korea (39368)

FDA FURLS Identifiers

FEI Number: 3013501671

Registration No: 3013501671 • Status Code: 1 (Active)

Designated U.S. Agent21 CFR 807.40

Soin Jung

Englewood Cliff, NJ (USA)

201-4722623

soin.jung@lge.com

Registered FDA Product Codes, Device Classes & Commercial Names

Cross-check your commercial invoice product descriptions against these active FDA product code filings to prevent NO_510K or UNAPPROVED_NEW_DRUG port holds.

Proprietary / Commercial Brand Names on File

27HJ713S
Product CodeFDA Classification NameDevice Class21 CFR Regulation510(k) Exempt?
GCJLaparoscope, General & Plastic SurgeryClass 221 CFR 876.1500 Requires 510(k) / Check
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Other Verified FDA FEI Establishments in South Korea

Frequently Asked Questions: FEI 3013501671 (LG ELECTRONICS INC.)

What is the FDA FEI Number for LG ELECTRONICS INC.?

According to public US FDA Establishment Registration records, LG ELECTRONICS INC. (Gumi-si Gyeongbuk, South Korea) is assigned FDA Facility Establishment Identifier (FEI) 3013501671 (Registration No. 3013501671) with registration year 2027.

Who is the designated US Agent for FEI 3013501671 (LG ELECTRONICS INC.)?

The registered US Agent on file for FEI 3013501671 is Soin Jung located in Englewood Cliff, NJ. Importers should independently confirm active representation before filing CBP ACE entry.

Does an active FDA FEI registration guarantee that shipments from LG ELECTRONICS INC. will clear US Customs without detention?

No. An active FDA FEI number or establishment registration only confirms administrative listing in FDA FURLS. Shipments can still be detained at US ports under Detention Without Physical Examination (DWPE / Import Alerts) for labeling, 510(k), cGMP, or adulteration violations.