Data / Medical devices / South Korea / Rgorithm Korea
Rgorithm Korea: FDA-registered device maker in Guemcheon-gu Seoul, South Korea, 1 510(k) clearance
Rgorithm Korea is registered with the FDA (registration 3029915447) in Guemcheon-gu Seoul, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 18, 2023. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3029915447
- Address
- #A 1502,1503, 606, seobusaet-gil, guemcheon-gu, Republic of Korea, Guemcheon-gu Seoul, South Korea, 08504
- Owner or operator
- Rgorithm Korea (10088456)
- Roles
- Manufacturer
- First device listed
- October 12, 2023
- Registered through
- 2027
- Brand names listed
- TRUST
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dental Abutment Design Software For Dental Laboratory | PNP | 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 |
|---|---|---|---|---|---|---|
| July 18, 2023 | K221107 | TRUST | PNP | Substantially Equivalent | Rgorithm Korea | accessdata.fda.gov |
Compare with other makers
Updated July 18, 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.