Data / Medical devices / Laparoscope, General & Plastic Surgery / South Korea
FDA-registered makers of Laparoscope, General & Plastic Surgery in South Korea: 5 establishments
5 establishments in South Korea are registered with the FDA to make Laparoscope, General & Plastic Surgery (product code GCJ). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Laparoscope, General & Plastic Surgery
- Product code
- GCJ
- Country
- South Korea
Makers of Laparoscope, General & Plastic Surgery in South Korea
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| LG Electronics Inc. | Gumi-si Gyeongbuk, South Korea | Exporter to the US, Manufacturer | 5 | July 17, 2026 | 0 | 0 | 0 | api.fda.gov |
| Incore Co., Ltd. | Daegu, South Korea | Manufacturer | 1 | June 21, 2022 | 0 | 0 | 0 | api.fda.gov |
| LivsMed Inc. | Seongnam-si Gyeonggi, South Korea | Manufacturer | 1 | December 3, 2021 | 0 | 0 | 0 | api.fda.gov |
| D&T Inc. | Yuseong-gu Daejeon, South Korea | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vpix Medical, Inc. | Jung-gu Daejeon, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.