Data / Medical devices / South Korea / LG Electronics Inc.
LG Electronics Inc.: FDA-registered device maker in Gumi-si Gyeongbuk, South Korea, 27 510(k) clearances
LG Electronics Inc. is registered with the FDA (registration 3013501671) in Gumi-si Gyeongbuk, South Korea. It lists 5 device types. The FDA files 27 510(k) clearances under its listings, the newest dated July 17, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013501671
- Address
- 168, Suchul-daero Gyeongsangbuk-do, Gumi-si Gyeongbuk, South Korea, 39368
- 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
- 10HQ701G-B, 10HQ701G-BP, 14HK701G-W, 14HK701G-WP, 14HQ701G-B, 14HQ701G-BP, 14HQ901G-B, 14HQ901G-BP and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Television, Surgical, Without Audio | FWB | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Display, Diagnostic Radiology | PGY | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Solid State X-Ray Imager (Flat Panel/Digital Imager) | MQB | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | Exporter to the US, Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 17, 2026 | K261614 | LED LCD Monitor (OEV-271H) | GCJ | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| June 12, 2026 | K261213 | Medical Monitor (40HT513D) | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| June 12, 2025 | K251209 | Medical Monitor (32HS710S) | GCJ | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| January 28, 2025 | K243439 | Medical Monitor (27HS714S) | GCJ | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| August 12, 2024 | K241402 | Medical Monitor (32HR734S) | GCJ | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| March 18, 2024 | K233599 | X-Clever (ASHK100G) | LLZ | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| February 15, 2024 | K240130 | Medical Monitor (21HQ613D) | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| December 11, 2023 | K232985 | 24HR513C | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| August 15, 2023 | K232127 | 21HQ513D, 32HL512D, 31HN713D, 32HQ713D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| April 27, 2023 | K230845 | 32HL512D, 31HN713D, 32HQ713D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| March 1, 2023 | K223423 | 32HQ713D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| January 9, 2023 | K223789 | 21HQ513D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| July 22, 2022 | K221461 | 10HQ701G-B | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| July 22, 2022 | K221394 | 14HQ701G-B | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| July 13, 2022 | K221434 | 17HQ701G-B | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| May 5, 2022 | K220559 | 17HQ901G-B | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| February 16, 2022 | K214044 | 14HQ901G-B | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| December 10, 2021 | K212137 | X-Clever | LLZ | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| December 3, 2021 | K212295 | 21HQ513D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| October 8, 2020 | K201777 | 31HN713D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| March 13, 2020 | K192925 | 32HL512D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| December 5, 2019 | K191864 | 21HK512D | PGY | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| May 30, 2019 | K191188 | ASHK100G | LLZ | Substantially Equivalent | Lg Electronics | accessdata.fda.gov |
| December 7, 2018 | K183286 | 17HK701G-W | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| October 18, 2018 | K182348 | 14HK701G-W | MQB | Substantially Equivalent | Lg Electronics.Inc | accessdata.fda.gov |
| June 8, 2018 | K180332 | 17HK700G-W | MQB | Substantially Equivalent | Lg Electronics | accessdata.fda.gov |
| May 30, 2017 | K170899 | 27HJ713S | GCJ | Substantially Equivalent | Lg Electronics | accessdata.fda.gov |
Compare with other makers
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Solid State X-Ray Imager (Flat Panel/Digital Imager)
- All makers of Display, Diagnostic Radiology
- All makers of Camera, Television, Surgical, Without Audio
- All makers of System, Image Processing, Radiological
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.