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Data / Medical devices / China / LG Electronics Nanjing New Technology Co., Ltd.

LG Electronics Nanjing New Technology Co., Ltd.: FDA-registered device maker in Nanjing Jiangsu, China, 16 510(k) clearances

LG Electronics Nanjing New Technology Co., Ltd. is registered with the FDA (registration 3004434200) in Nanjing Jiangsu, China. It lists 4 device types. The FDA files 16 510(k) clearances under its listings, the newest dated July 17, 2026. Registered through 2026. FDA data exported November 3, 2026.

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Get makers like this oneWatch LG Electronics Nanjing New Technology Co., Ltd.
FDA registration number
3004434200
Address
NO.346, Yaoxin Road, Economic & Technical Development Zone, Nanjing Jiangsu, China, 210038
Owner or operator
LG Electronics Inc Monitor Division. (10053135)
Roles
Exporter to the US, Manufacturer
First device listed
November 3, 2016
Registered through
2026
Brand names listed
19HK312C, 27HJ712C, 27HJ713C, 27HS713C, 21HK512D, 21HQ513D, 21HQ613D, 24CK560N, 24CN670NK, 24CN670WK, 24CN670IK, 24CR670NK, 24CR670WK, 24CR670IK, 24CR671NK, 24CR671WK, 24CR671IK, 24CR670W, 24HR513C and more

Devices it lists

DeviceProduct codeClassRoleSource
Camera, Television, Surgical, Without AudioFWB1Exporter to the US, Manufactureraccessdata.fda.gov
Display, Diagnostic RadiologyPGY2Exporter to the US, Manufactureraccessdata.fda.gov
Laparoscope, General & Plastic SurgeryGCJ2Exporter to the US, Manufactureraccessdata.fda.gov
System, Image Processing, RadiologicalLLZ2Exporter to the US, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 17, 2026K261614LED LCD Monitor (OEV-271H)GCJSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
June 12, 2026K261213Medical Monitor (40HT513D)PGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
June 12, 2025K251209Medical Monitor (32HS710S)GCJSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
January 28, 2025K243439Medical Monitor (27HS714S)GCJSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
August 12, 2024K241402Medical Monitor (32HR734S)GCJSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
February 15, 2024K240130Medical Monitor (21HQ613D)PGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
December 11, 2023K23298524HR513CPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
August 15, 2023K23212721HQ513D, 32HL512D, 31HN713D, 32HQ713DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
April 27, 2023K23084532HL512D, 31HN713D, 32HQ713DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
March 1, 2023K22342332HQ713DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
January 9, 2023K22378921HQ513DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
December 3, 2021K21229521HQ513DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
October 8, 2020K20177731HN713DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
March 13, 2020K19292532HL512DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
December 5, 2019K19186421HK512DPGYSubstantially EquivalentLg Electronics.Incaccessdata.fda.gov
May 30, 2017K17089927HJ713SGCJSubstantially EquivalentLg Electronicsaccessdata.fda.gov

Compare with other makers

Updated July 17, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.