Data / Medical devices / South Korea / Beacon Korea Inc.
Beacon Korea Inc.: FDA-registered device maker in Seongnam-si Gyeonggi, South Korea, 2 510(k) clearances
Beacon Korea Inc. is registered with the FDA (registration 3031232523) in Seongnam-si Gyeonggi, South Korea. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 28, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031232523
- Address
- #1501~1504, 37, Sagimakgol-ro 62beon-gil, Jungwon-gu, Seongnam-si Gyeonggi, South Korea, 13211
- Owner or operator
- BEACON KOREA INC. (10090748)
- Roles
- Manufacturer
- First device listed
- October 28, 2024
- Registered through
- 2026
- Brand names listed
- 8MP Color LCD Displays C811W, C811WT, PA27 and PA27T, LCD Monitors C310S G310S C316S G316S C616W
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Digital Pathology Display | PZZ | 2 | Manufacturer | accessdata.fda.gov |
| Display, Diagnostic Radiology | PGY | 2 | 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 |
|---|---|---|---|---|---|---|
| December 28, 2024 | K233119 | 8MP Color LCD Displays C811W, C811WT, PA27 and PA27T | PZZ | Substantially Equivalent | Shenzhen Beacon Display Technology Co., Ltd. | accessdata.fda.gov |
| October 25, 2024 | K243031 | LCD Monitors C310S, G310S, C316S, G316S, C616W | PGY | Substantially Equivalent | Shenzhen Beacon Display Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 28, 2024. 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.