Data / Medical devices / South Korea / maihub Corp.
maihub Corp.: FDA-registered device maker in Gangnam-gu Seoul, South Korea, 1 510(k) clearance
maihub Corp. is registered with the FDA (registration 3043532712) in Gangnam-gu Seoul, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 5, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043532712
- Address
- #503, 5F, 124 Teheran-ro, Gangnam-gu Seoul, South Korea, 06234
- Owner or operator
- maihub Corp. (10095010)
- Roles
- Manufacturer
- First device listed
- January 14, 2026
- Registered through
- 2026
- Brand names listed
- maiLink
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| January 5, 2026 | K253008 | maiLink | LLZ | Substantially Equivalent | Maihub Corp. | accessdata.fda.gov |
Compare with other makers
Updated January 5, 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.