Data / Medical devices / South Korea / Vectornate Korea Inc
Vectornate Korea Inc: FDA-registered device maker in Jangseong-gun Jeonnam, South Korea, 1 510(k) clearance
Vectornate Korea Inc is registered with the FDA (registration 3013245669) in Jangseong-gun Jeonnam, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 3, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013245669
- Address
- 56 Nanosandan 2-ro, Jangseong-gun Jeonnam, South Korea, 57247
- Owner or operator
- Vectornate Korea Inc (10074593)
- Roles
- Reprocessor, Specification developer
- First device listed
- June 17, 2026
- Registered through
- 2026
- Brand names listed
- STM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Culture Media, Non-Propagating Transport | JSM | 1 | Reprocessor, Specification developer | 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 |
|---|---|---|---|---|---|---|
| May 3, 2023 | K212743 | MedSchenker Smart Transport Medium (STM15-A/STM20-A/STM30-A/SCS30-A) System | JSM | Substantially Equivalent | Medschenker, Inc. | accessdata.fda.gov |
Compare with other makers
Updated May 3, 2023. 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.